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Volumn , Issue , 2009, Pages 117-153

Thermomorphic Catalysts

Author keywords

Catalyst polymer separation in polymerizations and atom transfer radical polymerization (ATRP); Designing heptane phase soluble support; Hydroformylation reactions under thermomorphic conditions; Lower critical solution temperature (an LCST); Phase separation process affecting catalyst reactivity and product catalyst separation; Temperature induced phase changes making thermomorphic catalysis interesting; Thermomorphic catalyst separation strategies; Thermomorphic catalysts; Thermomorphic catalysts, homogeneous catalysts and phase change; Thermoregulated phase transfer catalysis (TRPTC)

Indexed keywords


EID: 80051744343     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9780470682005.ch6     Document Type: Chapter
Times cited : (12)

References (116)
  • 1
    • 0016578214 scopus 로고
    • Preparation of films exhibiting a balanced temperature dependence to permeation by aqueous solution. Lower consolute behavior
    • L. D. Taylor and L. D. Cerankowski, Preparation of films exhibiting a balanced temperature dependence to permeation by aqueous solution. Lower consolute behavior, J. Polym. Sci., Polym. Chem. Ed., 13, 2551-2570 (1975).
    • (1975) J. Polym. Sci., Polym. Chem. Ed. , vol.13 , pp. 2551-2570
    • Taylor, L.D.1    Cerankowski, L.D.2
  • 2
    • 0032497209 scopus 로고    scopus 로고
    • Poly(N-isopropylacrylamide) soluble polymer supports in catalysis and synthesis
    • D. E. Bergbreiter, B. L. Case, Y. -S. Liu and J. W. Caraway, Poly(N-isopropylacrylamide) soluble polymer supports in catalysis and synthesis, Macromolecules, 31, 6053-6062 (1998).
    • (1998) Macromolecules , vol.31 , pp. 6053-6062
    • Bergbreiter, D.E.1    Case, B.L.2    Liu, Y.-S.3    Caraway, J.W.4
  • 4
    • 0029212754 scopus 로고
    • Polymer ligands that can regulate reaction temperature in 'smart' catalysts
    • D. E. Bergbreiter, V. M. Mariagnanam and L. Zhang, Polymer ligands that can regulate reaction temperature in 'smart' catalysts, Adv. Mater., 7, 69-71 (1995).
    • (1995) Adv. Mater. , vol.7 , pp. 69-71
    • Bergbreiter, D.E.1    Mariagnanam, V.M.2    Zhang, L.3
  • 5
    • 33749491911 scopus 로고
    • Smart ligands that regulate homogeneously catalyzed reactions
    • D. E. Bergbreiter, L. Zhang, and V. M. Mariagnanam, Smart ligands that regulate homogeneously catalyzed reactions, J. Am. Chem. Soc., 115, 9295-9296 (1993).
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 9295-9296
    • Bergbreiter, D.E.1    Zhang, L.2    Mariagnanam, V.M.3
  • 6
    • 0001701684 scopus 로고    scopus 로고
    • Homogenous enzymatic synthesis using a thermo-responsive water-soluble polymer support
    • X. Huang, K. L. Witte, D. E. Bergbreiter, and C. -H. Wong, Homogenous enzymatic synthesis using a thermo-responsive water-soluble polymer support, Adv. Synth. Catal., 343, 675-681 (2001).
    • (2001) Adv. Synth. Catal. , vol.343 , pp. 675-681
    • Huang, X.1    Witte, K.L.2    Bergbreiter, D.E.3    Wong, C.-H.4
  • 7
    • 0037453649 scopus 로고    scopus 로고
    • Smart aqueous reaction medium
    • D. M. Davies and E. L. Stringer, Smart aqueous reaction medium, Langmuir, 19, 1927-1928 (2003).
    • (2003) Langmuir , vol.19 , pp. 1927-1928
    • Davies, D.M.1    Stringer, E.L.2
  • 8
    • 37349092682 scopus 로고    scopus 로고
    • A new solid-phase reaction system utilizing a temperature-responsive catalyst: oxidative cyclization with hydrogen peroxide
    • H. Hamamoto, Y. Suzuki, H. Takahashi and S. Ikegami, A new solid-phase reaction system utilizing a temperature-responsive catalyst: oxidative cyclization with hydrogen peroxide, Adv. Synth. Catal., 349, 2685-2689 (2007).
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 2685-2689
    • Hamamoto, H.1    Suzuki, Y.2    Takahashi, H.3    Ikegami, S.4
  • 9
    • 61849172860 scopus 로고    scopus 로고
    • Designing surfaces with wettability that varies in response to solute identity and concentration
    • K. -S. Liao, H. Fu, A. Wan, J. D. Batteas, and D. E. Bergbreiter, Designing surfaces with wettability that varies in response to solute identity and concentration, Langmuir, 25, 26-29 (2009).
    • (2009) Langmuir , vol.25 , pp. 26-29
    • Liao, K.-S.1    Fu, H.2    Wan, A.3    Batteas, J.D.4    Bergbreiter, D.E.5
  • 10
    • 33748363102 scopus 로고    scopus 로고
    • Thermoregulated liquid/liquid catalyst separation and recycling
    • A. Behr, G. Henze, and R. Schomaecker, Thermoregulated liquid/liquid catalyst separation and recycling, Adv. Synth. Catal., 348, 1485-1495 (2006).
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 1485-1495
    • Behr, A.1    Henze, G.2    Schomaecker, R.3
  • 11
    • 50249091538 scopus 로고    scopus 로고
    • Multiphase catalysis in temperaturedependent multi-component solvent (TMS) systems
    • A. Behr, B. Turkowski, R. Roll, R. Schobel and G. Henze, Multiphase catalysis in temperaturedependent multi-component solvent (TMS) systems, Top. Organomet. Chem., 23, 19-52 (2008).
    • (2008) Top. Organomet. Chem. , vol.23 , pp. 19-52
    • Behr, A.1    Turkowski, B.2    Roll, R.3    Schobel, R.4    Henze, G.5
  • 12
    • 33748267496 scopus 로고    scopus 로고
    • Liquid/liquid biphasic recovery/reuse of soluble polymersupported catalysts
    • D. E. Bergbreiter and S. D. Sung, Liquid/liquid biphasic recovery/reuse of soluble polymersupported catalysts, Adv. Synth. Catal., 348, 1352-1366 (2006).
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 1352-1366
    • Bergbreiter, D.E.1    Sung, S.D.2
  • 13
    • 27944501154 scopus 로고    scopus 로고
    • Applications of catalysts on soluble supports
    • D. E. Bergbreiter and J. Li, Applications of catalysts on soluble supports, Top. Curr. Chem., 242, 113-176 (2004).
    • (2004) Top. Curr. Chem. , vol.242 , pp. 113-176
    • Bergbreiter, D.E.1    Li, J.2
  • 14
    • 0036811241 scopus 로고    scopus 로고
    • Using soluble polymers to recover catalysts and ligands
    • D. E. Bergbreiter, Using soluble polymers to recover catalysts and ligands, Chem. Rev., 102, 3345-3383 (2002).
    • (2002) Chem. Rev. , vol.102 , pp. 3345-3383
    • Bergbreiter, D.E.1
  • 16
    • 33947438481 scopus 로고
    • Liquid-liquid solubility of perfluoromethylcyclohexane with benzene, carbon tetrachloride, chlorobenzene, chloroform, and toluene
    • J. H. Hildebrand and D. R. F. Cochran, Liquid-liquid solubility of perfluoromethylcyclohexane with benzene, carbon tetrachloride, chlorobenzene, chloroform, and toluene, J. Am. Chem. Soc., 71, 22-25 (1949).
    • (1949) J. Am. Chem. Soc. , vol.71 , pp. 22-25
    • Hildebrand, J.H.1    Cochran, D.R.F.2
  • 17
    • 50249166579 scopus 로고    scopus 로고
    • PEG-modified ligands for catalysis and catalyst recycling in thermoregulated systems
    • E. Hermanns, J. Hasenjaeger, B. Driessen-Hoelscher, PEG-modified ligands for catalysis and catalyst recycling in thermoregulated systems, Top. Organometal. Chem., 23, 53-66 (2008).
    • (2008) Top. Organometal. Chem. , vol.23 , pp. 53-66
    • Hermanns, E.1    Hasenjaeger, J.2    Driessen-Hoelscher, B.3
  • 18
    • 65249112348 scopus 로고    scopus 로고
    • Biphasic catalysis with thermoregulated ligands
    • Z. Jin, Y. Wang, J. Jiang, and F. Wen, Biphasic catalysis with thermoregulated ligands, Curr. Top. Catal., 3, 15-32 (2002).
    • (2002) Curr. Top. Catal. , vol.3 , pp. 15-32
    • Jin, Z.1    Wang, Y.2    Jiang, J.3    Wen, F.4
  • 19
    • 0003476436 scopus 로고    scopus 로고
    • Thermoregulated phase-transfer catalysisin Aqueous-Phase Organometallic Catalysis
    • B. Cornils and W. A. Herrmann, Eds., Wiley, Weinheim
    • Z. Jin and X. Zheng, Thermoregulated phase-transfer catalysisin Aqueous-Phase Organometallic Catalysis, B. Cornils and W. A. Herrmann, Eds., Wiley, Weinheim, pp. 233-240 (1998).
    • (1998) , pp. 233-240
    • Jin, Z.1    Zheng, X.2
  • 20
    • 50249144569 scopus 로고    scopus 로고
    • Temperature-controlled catalyst recycling: new protocols based upon temperature-dependent solubilities of fluorous compounds and solid/liquid phase separations
    • J. A. Gladysz, and V. Tesevic, Temperature-controlled catalyst recycling: new protocols based upon temperature-dependent solubilities of fluorous compounds and solid/liquid phase separations, Top. Organometal. Chem., 23, 67-89 (2008).
    • (2008) Top. Organometal. Chem. , vol.23 , pp. 67-89
    • Gladysz, J.A.1    Tesevic, V.2
  • 21
    • 0000077126 scopus 로고    scopus 로고
    • Thermomorphic rhodium(I) and palladium(0) catalysts
    • D. E. Bergbreiter, Y. -S. Liu, and P. L. Osburn, Thermomorphic rhodium(I) and palladium(0) catalysts, J. Am. Chem. Soc., 120, 4250-4251 (1998).
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 4250-4251
    • Bergbreiter, D.E.1    Liu, Y.-S.2    Osburn, P.L.3
  • 23
    • 34547211263 scopus 로고    scopus 로고
    • A combinatorial approach to studying the effects of N-alkyl groups on poly(N-alkyl and N, N-dialkylacrylamide) Solubility
    • D. E. Bergbreiter, N. A. Aviles-Ramos, and D. Ortiz-Acosta, A combinatorial approach to studying the effects of N-alkyl groups on poly(N-alkyl and N, N-dialkylacrylamide) Solubility, J. Comb. Chem., 9, 609-617 (2007).
    • (2007) J. Comb. Chem. , vol.9 , pp. 609-617
    • Bergbreiter, D.E.1    Aviles-Ramos, N.A.2    Ortiz-Acosta, D.3
  • 24
    • 0015446074 scopus 로고
    • Pharmacologically active polymers. Model reactions for synthesis of pharmacologically active polymers by way of monomeric and polymeric reactive esters
    • H. G. Batz, G. Franzmann, and H. Ringsdorf, Pharmacologically active polymers. Model reactions for synthesis of pharmacologically active polymers by way of monomeric and polymeric reactive esters, Angew. Chem., Int. Ed. Engl., 11, 1103-1104 (1972).
    • (1972) Angew. Chem., Int. Ed. Engl. , vol.11 , pp. 1103-1104
    • Batz, H.G.1    Franzmann, G.2    Ringsdorf, H.3
  • 25
    • 33845247974 scopus 로고    scopus 로고
    • Synthesis, characterization, and utility of thermoresponsive natural/unnatural product macroligands for affinity chromatography
    • M. Zhou, A. Sivaramakrishnan, K. Ponnamperuma, Krishan, W. -K. Low, C. Li, J. O. Liu, D. E. Bergbreiter and D. Romo, Synthesis, characterization, and utility of thermoresponsive natural/unnatural product macroligands for affinity chromatography, Org. Lett., 8, 5247-5250 (2006).
    • (2006) Org. Lett. , vol.8 , pp. 5247-5250
    • Zhou, M.1    Sivaramakrishnan, A.2    Ponnamperuma, K.3    Krishan, W.-K.L.4    Li, C.5    Liu, J.O.6    Bergbreiter, D.E.7    Romo, D.8
  • 26
    • 10844225895 scopus 로고    scopus 로고
    • Dye-labeled PNIPAM [poly(N-isopropylacrylamide)]-supported acylation catalysts
    • C. Li and D. E. Bergbreiter, Dye-labeled PNIPAM [poly(N-isopropylacrylamide)]-supported acylation catalysts, Chem. Ind., 89, 545-550 (2003).
    • (2003) Chem. Ind. , vol.89 , pp. 545-550
    • Li, C.1    Bergbreiter, D.E.2
  • 27
    • 0030059084 scopus 로고    scopus 로고
    • Thermoresponsive polymer-bound substrates
    • D. E. Bergbreiter and J. W. Caraway, Thermoresponsive polymer-bound substrates, J. Am. Chem. Soc., 118, 6092-6093 (1996).
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 6092-6093
    • Bergbreiter, D.E.1    Caraway, J.W.2
  • 28
    • 0035823951 scopus 로고    scopus 로고
    • Nonpolar polymers for metal sequestration and ligand and catalyst recovery in thermomorphic systems
    • D. E. Bergbreiter, P. L. Osburn, and J. D. Frels, Nonpolar polymers for metal sequestration and ligand and catalyst recovery in thermomorphic systems, J. Am. Chem. Soc., 123, 11105-11106 (2001).
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 11105-11106
    • Bergbreiter, D.E.1    Osburn, P.L.2    Frels, J.D.3
  • 29
    • 0034721443 scopus 로고    scopus 로고
    • Palladium-catalyzed C-C coupling under thermomorphic conditions
    • D. E. Bergbreiter, P. L. Osburn, A. Wilson, and E. M. Sink, Palladium-catalyzed C-C coupling under thermomorphic conditions, J. Am. Chem. Soc., 122, 9058-9064 (2000).
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9058-9064
    • Bergbreiter, D.E.1    Osburn, P.L.2    Wilson, A.3    Sink, E.M.4
  • 30
    • 3242791617 scopus 로고    scopus 로고
    • Microwave-promoted Heck reactions using an oligo(ethyleneglycol)-bound SCS palladacycle under thermomorphic conditions
    • D. E. Bergbreiter and S. Furyk, Microwave-promoted Heck reactions using an oligo(ethyleneglycol)-bound SCS palladacycle under thermomorphic conditions, Green Chem., 6, 280-285 (2004).
    • (2004) Green Chem , vol.6 , pp. 280-285
    • Bergbreiter, D.E.1    Furyk, S.2
  • 31
    • 0001598367 scopus 로고
    • Functionalized ethylene oligomers as phase-transfer catalysts
    • D. E. Bergbreiter and J. R. Blanton, Functionalized ethylene oligomers as phase-transfer catalysts, J. Org. Chem., 50, 5828-5833 (1985).
    • (1985) J. Org. Chem. , vol.50 , pp. 5828-5833
    • Bergbreiter, D.E.1    Blanton, J.R.2
  • 32
    • 0001572344 scopus 로고
    • Recyclable polymer-bound lanthanide diene polymerization catalysts
    • D. E. Bergbreiter, L. -B. Chen and R. Chandran, Recyclable polymer-bound lanthanide diene polymerization catalysts, Macromolecules, 18, 1055-1057 (1985).
    • (1985) Macromolecules , vol.18 , pp. 1055-1057
    • Bergbreiter, D.E.1    Chen, L.-B.2    Chandran, R.3
  • 33
    • 0000199386 scopus 로고
    • Concurrent catalytic reduction/stoichiometric oxidation using oligomerically ligated catalysts and polymer-bound reagents
    • D. E. Bergbreiter and R. Chandran, Concurrent catalytic reduction/stoichiometric oxidation using oligomerically ligated catalysts and polymer-bound reagents, J. Am. Chem. Soc., 107, 4792-4793 (1985).
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 4792-4793
    • Bergbreiter, D.E.1    Chandran, R.2
  • 34
    • 0000211375 scopus 로고
    • Use of functionalized ethylene oligomers to prepare recoverable, recyclable nickel(0) diene cyclooligomerization catalysts
    • D. E. Bergbreiter and R. Chandran, Use of functionalized ethylene oligomers to prepare recoverable, recyclable nickel(0) diene cyclooligomerization catalysts, J. Org. Chem., 51, 4754-4760 (1986).
    • (1986) J. Org. Chem. , vol.51 , pp. 4754-4760
    • Bergbreiter, D.E.1    Chandran, R.2
  • 35
    • 33845281025 scopus 로고
    • Polyethylene-bound rhodium(I) hydrogenation catalysts
    • D. E. Bergbreiter and R. Chandran, Polyethylene-bound rhodium(I) hydrogenation catalysts, J. Am. Chem. Soc., 109, 174-179 (1987).
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 174-179
    • Bergbreiter, D.E.1    Chandran, R.2
  • 36
    • 33845183153 scopus 로고
    • Polyethylene-bound soluble recoverable palladium(0) catalysts
    • D. E. Bergbreiter and D. A. Weatherford, Polyethylene-bound soluble recoverable palladium(0) catalysts, J. Org. Chem., 54, 2726-2730 (1989).
    • (1989) J. Org. Chem. , vol.54 , pp. 2726-2730
    • Bergbreiter, D.E.1    Weatherford, D.A.2
  • 37
    • 0026889006 scopus 로고
    • New strategies in using macromolecular catalysts in organic synthesis
    • D. E. Bergbreiter, B. Chen, and D. Weatherford, New strategies in using macromolecular catalysts in organic synthesis, J. Mol. Catal., 74, 409-419 (1992).
    • (1992) J. Mol. Catal. , vol.74 , pp. 409-419
    • Bergbreiter, D.E.1    Chen, B.2    Weatherford, D.3
  • 38
    • 0000392533 scopus 로고
    • Soluble polyethylene-and polystyrene-bound tin halides as catalysts for reductions of alkyl and aryl bromides and iodides by sodium borohydride
    • D. E. Bergbreiter and S. A. Walker, Soluble polyethylene-and polystyrene-bound tin halides as catalysts for reductions of alkyl and aryl bromides and iodides by sodium borohydride, J. Org. Chem., 54, 5138-5141 (1989).
    • (1989) J. Org. Chem. , vol.54 , pp. 5138-5141
    • Bergbreiter, D.E.1    Walker, S.A.2
  • 39
    • 0000079450 scopus 로고
    • A polyethylene-bound ruthenium(II) catalyst for inter-and intramolecular Kharasch reactions
    • J. C. Phelps, D. E. Bergbreiter, G. M. Lee, R. Villani and S. M. Weinreb, A polyethylene-bound ruthenium(II) catalyst for inter-and intramolecular Kharasch reactions, Tet. Lett., 30, 3915-3918 (1989).
    • (1989) Tet. Lett. , vol.30 , pp. 3915-3918
    • Phelps, J.C.1    Bergbreiter, D.E.2    Lee, G.M.3    Villani, R.4    Weinreb, S.M.5
  • 40
    • 0025441521 scopus 로고
    • Polyethylene carboxylate-bound triruthenium clusters as alcohol oxidation catalysts
    • D. E. Bergbreiter and D. R. Treadwell, Polyethylene carboxylate-bound triruthenium clusters as alcohol oxidation catalysts, Reac. Polym., 12, 291-295 (1990).
    • (1990) Reac. Polym. , vol.12 , pp. 291-295
    • Bergbreiter, D.E.1    Treadwell, D.R.2
  • 42
    • 0034599359 scopus 로고    scopus 로고
    • Polyhomologation: the living polymerization of ylides
    • K. J. Shea, Polyhomologation: the living polymerization of ylides, Chem. -Eur. J., 6, 1113-1119 (2000).
    • (2000) Chem. -Eur. J. , vol.6 , pp. 1113-1119
    • Shea, K.J.1
  • 43
    • 84889404455 scopus 로고    scopus 로고
    • Baker-Petrolite sells terminally functionalized polyolefins with hydroxyl-and carboxylic acid groups under the tradenames UNILIN and UNICID
    • Baker-Petrolite sells terminally functionalized polyolefins with hydroxyl-and carboxylic acid groups under the tradenames UNILIN and UNICID.
  • 44
    • 33645506118 scopus 로고    scopus 로고
    • Thermomorphic system with non-fluorous phase-tagged Ru(BINAP) catalyst: Facile liquid/solid catalyst separation and application in asymmetric hydrogenation
    • Y. Y. Huang, Y. M. He, H. F. Zhou, L. Wu, B. L. Li, and Q. H. Fan, Thermomorphic system with non-fluorous phase-tagged Ru(BINAP) catalyst: Facile liquid/solid catalyst separation and application in asymmetric hydrogenation, J. Org. Chem., 71, 2874-2877 (2006).
    • (2006) J. Org. Chem. , vol.71 , pp. 2874-2877
    • Huang, Y.Y.1    He, Y.M.2    Zhou, H.F.3    Wu, L.4    Li, B.L.5    Fan, Q.H.6
  • 45
    • 17844373530 scopus 로고    scopus 로고
    • Palladium-platinum bimetallic nanoparticle catalysts using dendron assembly for selective hydrogenation of dienes and their application to thermomorphic system
    • M. Murata, Y. Tanaka, T. Mizugaki, K. Ebitani, K. Kaneda, Palladium-platinum bimetallic nanoparticle catalysts using dendron assembly for selective hydrogenation of dienes and their application to thermomorphic system, Chem. Lett., 34, 272-273 (2005).
    • (2005) Chem. Lett. , vol.34 , pp. 272-273
    • Murata, M.1    Tanaka, Y.2    Mizugaki, T.3    Ebitani, K.4    Kaneda, K.5
  • 46
    • 0034867043 scopus 로고    scopus 로고
    • Dendrimer-encapsulated metal nanoparticles: synthesis, characterization, and applications to catalysis
    • R. M. Crooks, M. Zhao, L. Sun, V. Checkhik, L. K. Yeung, Dendrimer-encapsulated metal nanoparticles: synthesis, characterization, and applications to catalysis, Acc. Chem. Res., 34, 181-190 (2001).
    • (2001) Acc. Chem. Res. , vol.34 , pp. 181-190
    • Crooks, R.M.1    Zhao, M.2    Sun, L.3    Checkhik, V.4    Yeung, L.K.5
  • 47
    • 0242691105 scopus 로고    scopus 로고
    • Dendrimer-encapsulated metal nanoparticles and their applications to catalysis
    • N. Niu and R. M. Crooks, Dendrimer-encapsulated metal nanoparticles and their applications to catalysis, Comptes Rendus Chim., 6, 1049-1059 (2003).
    • (2003) Comptes Rendus Chim. , vol.6 , pp. 1049-1059
    • Niu, N.1    Crooks, R.M.2
  • 48
    • 13244287959 scopus 로고    scopus 로고
    • Synthesis, characterization, and applications of dendrimer-encapsulated nanoparticles
    • R. W. J. Scott, O. M. Wilson, and R. M. Crooks, Synthesis, characterization, and applications of dendrimer-encapsulated nanoparticles, J. Phys. Chem., B, 109, 692-704 (2005).
    • (2005) J. Phys. Chem., B , vol.109 , pp. 692-704
    • Scott, R.W.J.1    Wilson, O.M.2    Crooks, R.M.3
  • 50
    • 37549058419 scopus 로고    scopus 로고
    • PEG-stabilized palladium nanoparticles: An efficient and recyclable catalyst for the selective hydrogenation of 1, 5-cyclooctadiene in thermoregulated PEG biphase system
    • T. S. Huang, Y. H. Wang, J. Y. Jiang, Z. L. Jin, PEG-stabilized palladium nanoparticles: An efficient and recyclable catalyst for the selective hydrogenation of 1, 5-cyclooctadiene in thermoregulated PEG biphase system, Chin. Chem. Lett., 19, 102-104 (2008).
    • (2008) Chin. Chem. Lett. , vol.19 , pp. 102-104
    • Huang, T.S.1    Wang, Y.H.2    Jiang, J.Y.3    Jin, Z.L.4
  • 51
    • 0037452822 scopus 로고    scopus 로고
    • Thermoregulated phase-separable phosphine ruthenium complex for hydrogenation catalysis
    • Y. Wang, X. Wu, F. Cheng, and Z. Jin, Thermoregulated phase-separable phosphine ruthenium complex for hydrogenation catalysis, J. Mol. Catal. A. : Chem., 195, 133-137 (2003).
    • (2003) J. Mol. Catal. A. : Chem. , vol.195 , pp. 133-137
    • Wang, Y.1    Wu, X.2    Cheng, F.3    Jin, Z.4
  • 52
    • 0141563346 scopus 로고    scopus 로고
    • Highly selective tandem isomerization-hydroformylation reaction of trans-4-octene to n-nonanal with rhodium-BIPHEPHOS catalysis
    • A. Behr, D. Obst, C. Schulte, and T. Schosser, Highly selective tandem isomerization-hydroformylation reaction of trans-4-octene to n-nonanal with rhodium-BIPHEPHOS catalysis, J. Mol. Catal., A: Chem., 206, 179-184 (2003).
    • (2003) J. Mol. Catal., A: Chem. , vol.206 , pp. 179-184
    • Behr, A.1    Obst, D.2    Schulte, C.3    Schosser, T.4
  • 53
    • 11144251835 scopus 로고    scopus 로고
    • Isomerizing hydroformylation of trans-4-octene to n-nonanal in multiphase systems: acceleration effect of propylene carbonate
    • A. Behr, D. Obst, and B. Turkowski, Isomerizing hydroformylation of trans-4-octene to n-nonanal in multiphase systems: acceleration effect of propylene carbonate, J. Mol. Catal., A: Chem., 226, 215-219 (2005).
    • (2005) J. Mol. Catal., A: Chem. , vol.226 , pp. 215-219
    • Behr, A.1    Obst, D.2    Turkowski, B.3
  • 54
    • 24944586823 scopus 로고    scopus 로고
    • Selection process of newsolvents in temperaturedependent multi-component solvent systems and its application in isomerising hydroformylation
    • A. Behr, G. Henze, B. Turkowski, and D. Obst, Selection process of newsolvents in temperaturedependent multi-component solvent systems and its application in isomerising hydroformylation, Green Chem., 7, 645-649 (2005).
    • (2005) Green Chem. , vol.7 , pp. 645-649
    • Behr, A.1    Henze, G.2    Turkowski, B.3    Obst, D.4
  • 55
    • 43049176372 scopus 로고    scopus 로고
    • Solubility of carbon monoxide and hydrogen in propylene carbonate and thermomorphic multicomponent hydroformylation solvent
    • M. S. Shaharun, H. Mukhtar, and B. K. Dutta, Solubility of carbon monoxide and hydrogen in propylene carbonate and thermomorphic multicomponent hydroformylation solvent, Chem. Eng. Sci., 63, 3024-3035 (2008).
    • (2008) Chem. Eng. Sci. , vol.63 , pp. 3024-3035
    • Shaharun, M.S.1    Mukhtar, H.2    Dutta, B.K.3
  • 56
    • 33646013868 scopus 로고    scopus 로고
    • Selective thermomorphic biphasic hydroformylation of higher olefins catalyzed by HRhCO(PPh3)3/P(OPh)3
    • J. Tijani and B. El Ali, Selective thermomorphic biphasic hydroformylation of higher olefins catalyzed by HRhCO(PPh3)3/P(OPh)3, Appl. Catal. A: General, 303, 158-165 (2006).
    • (2006) Appl. Catal. A: General , vol.303 , pp. 158-165
    • Tijani, J.1    El Ali, B.2
  • 57
    • 0028116495 scopus 로고
    • Facile catalyst separation without water: fluorous biphase hydroformylation of olefins
    • I. T. Horvath and J. Rabai, Facile catalyst separation without water: fluorous biphase hydroformylation of olefins, Science, 266, 72-75 (1994).
    • (1994) Science , vol.266 , pp. 72-75
    • Horvath, I.T.1    Rabai, J.2
  • 58
    • 0033481596 scopus 로고    scopus 로고
    • Fluorous phase separation techniques in catalysis
    • E. de Wolf, G. van Koten, B. -J. Deelman, Fluorous phase separation techniques in catalysis, Chem. Soc. Rev., 28, 37-41 (1999).
    • (1999) Chem. Soc. Rev. , vol.28 , pp. 37-41
    • De Wolf, E.1    Van Koten, G.2    Deelman, B.-J.3
  • 59
    • 2942545969 scopus 로고    scopus 로고
    • Fluorous Synthesis of heterocyclic systems
    • W. Zhang, Fluorous Synthesis of heterocyclic systems, Chem. Rev., 104, 2531-2556 (2004).
    • (2004) Chem. Rev. , vol.104 , pp. 2531-2556
    • Zhang, W.1
  • 60
    • 34447135655 scopus 로고    scopus 로고
    • Biocatalysis in supercritical fluids, in fluorous solvents, and under solvent-free conditions
    • H. R. Hobbs and N. R. Thomas, Biocatalysis in supercritical fluids, in fluorous solvents, and under solvent-free conditions, Chem. Rev., 107, 2786-2820 (2007).
    • (2007) Chem. Rev. , vol.107 , pp. 2786-2820
    • Hobbs, H.R.1    Thomas, N.R.2
  • 61
    • 0345255621 scopus 로고    scopus 로고
    • Aqueous biphasic catalysis as a powerful tool for catalyst recycling in telomerization and hydrogenation chemistry
    • A. Behr, M. Urschey, and V. A. Brehme, Aqueous biphasic catalysis as a powerful tool for catalyst recycling in telomerization and hydrogenation chemistry, Green Chem., 5, 198-204 (2003).
    • (2003) Green Chem. , vol.5 , pp. 198-204
    • Behr, A.1    Urschey, M.2    Brehme, V.A.3
  • 62
    • 0001195653 scopus 로고    scopus 로고
    • A soluble fluorous phase polymer support
    • D. E. Bergbreiter and J. G. Franchina, A soluble fluorous phase polymer support, Chem. Commun., 1531-1532 (1997).
    • (1997) Chem. Commun. , pp. 1531-1532
    • Bergbreiter, D.E.1    Franchina, J.G.2
  • 64
    • 0000072244 scopus 로고    scopus 로고
    • Fluoroacrylate-bound fluorous-phase soluble hydrogenation catalysts
    • D. E. Bergbreiter, J. G. Franchina, and B. L. Case, Fluoroacrylate-bound fluorous-phase soluble hydrogenation catalysts, Org. Lett., 2, 393-395 (2000).
    • (2000) Org. Lett. , vol.2 , pp. 393-395
    • Bergbreiter, D.E.1    Franchina, J.G.2    Case, B.L.3
  • 65
    • 0034678077 scopus 로고    scopus 로고
    • Sequestration of trace metals using water-soluble and fluorous phase-soluble polymers
    • D. E. Bergbreiter, N. Koshti, J. G. Franchina, and J. D. Frels, Sequestration of trace metals using water-soluble and fluorous phase-soluble polymers, Angew. Chem., Int. Ed., 39, 1040-1042 (2000).
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 1040-1042
    • Bergbreiter, D.E.1    Koshti, N.2    Franchina, J.G.3    Frels, J.D.4
  • 66
    • 0034697473 scopus 로고    scopus 로고
    • Fluorous soluble polymer catalysts for the fluorous biphase hydroformylation of olefins
    • W. Chen, L. Xu, and J. Xiao, Fluorous soluble polymer catalysts for the fluorous biphase hydroformylation of olefins, Chem. Commun., 839-840 (2000s).
    • (2000) Chem. Commun. , pp. 839-840
    • Chen, W.1    Xu, L.2    Xiao, J.3
  • 67
    • 5144223766 scopus 로고    scopus 로고
    • Hydroformylation of styrene in supercritical carbon dioxide with fluoroacrylate polymer supported rhodium catalysts
    • I. Kani, R. Flores, J. P. Fackler, and A. Akgerman, Hydroformylation of styrene in supercritical carbon dioxide with fluoroacrylate polymer supported rhodium catalysts, J. Supercrit. Fluids, 31, 287-294 (2004).
    • (2004) J. Supercrit. Fluids , vol.31 , pp. 287-294
    • Kani, I.1    Flores, R.2    Fackler, J.P.3    Akgerman, A.4
  • 68
    • 0346907124 scopus 로고    scopus 로고
    • Kinetics of the Homogeneous catalytic Hydrogenation of olefins in supercritical carbon dioxide using a fluoroacrylate copolymer grafted rhodium catalyst
    • R. Flores, Z. K. Lopez-Castillo, I. Kani, J. P. Fackler, Jr., and A. Akgerman, Kinetics of the Homogeneous catalytic Hydrogenation of olefins in supercritical carbon dioxide using a fluoroacrylate copolymer grafted rhodium catalyst, Ind. Eng. Chem. Res., 42, 6720-6729 (2003).
    • (2003) Ind. Eng. Chem. Res. , vol.42 , pp. 6720-6729
    • Flores, R.1    Lopez-Castillo, Z.K.2    Kani, I.3    Fackler Jr., J.P.4    Akgerman, A.5
  • 69
    • 0041470351 scopus 로고    scopus 로고
    • Evaluation of polymer-supported Rhodium catalysts in 1-octene hydroformylation in supercritical carbon Dioxide
    • Z. K. Lopez-Castillo, R. Flores, I. Kani, J. P. Fackler, Jr., and A. Akgerman, Evaluation of polymer-supported Rhodium catalysts in 1-octene hydroformylation in supercritical carbon Dioxide, Ind. Eng. Chem. Res., 42, 3893-3899 (2003).
    • (2003) Ind. Eng. Chem. Res. , vol.42 , pp. 3893-3899
    • Lopez-Castillo, Z.K.1    Flores, R.2    Kani, I.3    Fackler Jr., J.P.4    Akgerman, A.5
  • 70
    • 0037178077 scopus 로고    scopus 로고
    • Fluoroacrylate copolymer-supported Rhodium catalysts for hydrogenation reactions in supercritical carbon dioxide
    • Z. K. Lopez-Castillo, R. Flores, I. Kani, J. P. Fackler, Jr., and A. Akgerman, Fluoroacrylate copolymer-supported Rhodium catalysts for hydrogenation reactions in supercritical carbon dioxide, Ind. Eng. Chem. Res., 41, 3075-3080 (2002).
    • (2002) Ind. Eng. Chem. Res. , vol.41 , pp. 3075-3080
    • Lopez-Castillo, Z.K.1    Flores, R.2    Kani, I.3    Fackler Jr., J.P.4    Akgerman, A.5
  • 71
    • 4143115584 scopus 로고    scopus 로고
    • Biphasic hydroformylation of higher olefins
    • AIChE Spring National Meeting, Conference Proceedings, New Orleans, LA, US, Apr. 25-29
    • D. Dietz, C. Ohman, and T. Scholten, Biphasic hydroformylation of higher olefins, in AIChE Spring National Meeting, Conference Proceedings, New Orleans, LA, US, Apr. 25-29, 2004, pp. 309-313.
    • (2004) , pp. 309-313
    • Dietz, D.1    Ohman, C.2    Scholten, T.3
  • 72
    • 0031042062 scopus 로고    scopus 로고
    • Thermoregulated phase transfer ligands and catalysis. I. Synthesis of novel polyether-substituted triphenylphosphines and application of their rhodium complexes in two-phase hydroformylation
    • Z. Jin, X. Zheng, and B. Fell, Thermoregulated phase transfer ligands and catalysis. I. Synthesis of novel polyether-substituted triphenylphosphines and application of their rhodium complexes in two-phase hydroformylation, J. Mol. Cat., A: Chem., 116, 55-58 (1997).
    • (1997) J. Mol. Cat., A: Chem. , vol.116 , pp. 55-58
    • Jin, Z.1    Zheng, X.2    Fell, B.3
  • 73
    • 0037092937 scopus 로고    scopus 로고
    • Thermoregulated phase transfer ligands and catalysis. Part XIII. Use of nonionic tensioactive water-soluble phosphine ligands to effect homogeneous catalyst separation and recycling
    • Y. Wang, J. Jiang, Q. Miao, X. Wu, and Z. Jin, Thermoregulated phase transfer ligands and catalysis. Part XIII. Use of nonionic tensioactive water-soluble phosphine ligands to effect homogeneous catalyst separation and recycling, Catal. Today, 74, 85-90 (2002).
    • (2002) Catal. Today , vol.74 , pp. 85-90
    • Wang, Y.1    Jiang, J.2    Miao, Q.3    Wu, X.4    Jin, Z.5
  • 74
    • 0000371274 scopus 로고    scopus 로고
    • Thermoregulated phase-transfer ligands and catalysis. Part VI. Twophase hydroformylation of styrene catalyzed by the thermoregulated phase-transfer catalyst OPGPP/Rh
    • R. Chen, X. Liu, and Z. Jin, Thermoregulated phase-transfer ligands and catalysis. Part VI. Twophase hydroformylation of styrene catalyzed by the thermoregulated phase-transfer catalyst OPGPP/Rh, J. Organomet. Chem., 571, 201-204 (1998).
    • (1998) J. Organomet. Chem. , vol.571 , pp. 201-204
    • Chen, R.1    Liu, X.2    Jin, Z.3
  • 75
    • 0037655007 scopus 로고    scopus 로고
    • Thermoregulated phase transfer ligands and catalysis. XVIII: Synthesis of N, N-dipolyoxyethylene-substituted-2-(diphenylphosphino)-phenylamine (PEO-DPPPA) and the catalytic activity of its rhodium complex in the aqueous-organic biphasic hydroformylation of 1-decene
    • C. Liu, J. Jiang, Y. Wang, F. Cheng, and Z. Jin, Thermoregulated phase transfer ligands and catalysis. XVIII: Synthesis of N, N-dipolyoxyethylene-substituted-2-(diphenylphosphino)-phenylamine (PEO-DPPPA) and the catalytic activity of its rhodium complex in the aqueous-organic biphasic hydroformylation of 1-decene, J. Mol. Cat., A: Chem., 198, 23-27 (2003).
    • (2003) J. Mol. Cat., A: Chem. , vol.198 , pp. 23-27
    • Liu, C.1    Jiang, J.2    Wang, Y.3    Cheng, F.4    Jin, Z.5
  • 76
    • 23444436410 scopus 로고    scopus 로고
    • Hydroaminomethylation in thermomorphic solvent systems
    • A. Behr and R. Roll, Hydroaminomethylation in thermomorphic solvent systems, J. Mol. Catal. A: Chem., 239, 180-184 (2005).
    • (2005) J. Mol. Catal. A: Chem. , vol.239 , pp. 180-184
    • Behr, A.1    Roll, R.2
  • 77
    • 1242336838 scopus 로고    scopus 로고
    • Supramolecular catalysts by encapsulating palladium complexes within dendrimers
    • M. Ooe, M. Murata, T. Mizugaki, K. Ebitani and K. Kaneda, Supramolecular catalysts by encapsulating palladium complexes within dendrimers, J. Am. Chem. Soc., 126, 1604-1605 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 1604-1605
    • Ooe, M.1    Murata, M.2    Mizugaki, T.3    Ebitani, K.4    Kaneda, K.5
  • 78
    • 0037033366 scopus 로고    scopus 로고
    • Novel catalysis of dendrimer-bound Pd(0) complexes: sterically steered allylic amination and the first application for a thermomorphic system
    • T. Mizugaki, M. Murata, M. Ooe, K. Ebitani and K. Kaneda, Novel catalysis of dendrimer-bound Pd(0) complexes: sterically steered allylic amination and the first application for a thermomorphic system, Chem. Commun., 52-53 (2002).
    • (2002) Chem. Commun. , pp. 52-53
    • Mizugaki, T.1    Murata, M.2    Ooe, M.3    Ebitani, K.4    Kaneda, K.5
  • 79
    • 0032748890 scopus 로고    scopus 로고
    • Tridentate SCS Palladium(II) complexes: new, highly stable, recyclable catalysts for the Heck reaction
    • D. E. Bergbreiter, P. L. Osburn, and Y. -S. Liu, Tridentate SCS Palladium(II) complexes: new, highly stable, recyclable catalysts for the Heck reaction, J. Am. Chem. Soc., 121, 9531-9538 (1999).
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9531-9538
    • Bergbreiter, D.E.1    Osburn, P.L.2    Liu, Y.-S.3
  • 80
    • 14644438518 scopus 로고    scopus 로고
    • Evidence that SCS pincer Pd(II) complexes are only precatalysts in Heck catalysis and the implications for catalyst recovery and reuse
    • K. Q. Yu, W. Sommer, J. M. Richardson, M. Weck, and C. W. Jones, Evidence that SCS pincer Pd(II) complexes are only precatalysts in Heck catalysis and the implications for catalyst recovery and reuse, Adv. Synth. Catal., 347, 161-171 (2005).
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 161-171
    • Yu, K.Q.1    Sommer, W.2    Richardson, J.M.3    Weck, M.4    Jones, C.W.5
  • 82
    • 14644433669 scopus 로고    scopus 로고
    • Mechanistic studies of SCS-Pd complexes used in Heck catalysis
    • D. E. Bergbreiter, P. L. Osburn, and J. D. Frels, Mechanistic studies of SCS-Pd complexes used in Heck catalysis, Adv. Synth. Catal., 347, 172-184.
    • Adv. Synth. Catal. , vol.347 , pp. 172-184
    • Bergbreiter, D.E.1    Osburn, P.L.2    Frels, J.D.3
  • 83
    • 0001489150 scopus 로고    scopus 로고
    • Highly active thermomorphic fluorous palladacycle catalyst precursors for the Heck reaction; evidence for a palladium nanoparticle pathway
    • C. Rocaboy and J. A. Gladysz, Highly active thermomorphic fluorous palladacycle catalyst precursors for the Heck reaction; evidence for a palladium nanoparticle pathway, Org. Lett., 4, 1993-1996 (2002).
    • (2002) Org. Lett. , vol.4 , pp. 1993-1996
    • Rocaboy, C.1    Gladysz, J.A.2
  • 84
    • 0037241661 scopus 로고    scopus 로고
    • Thermomorphic fluorous imine and thioether palladacycles as precursors for highly active Heck and Suzuki catalysts; evidence for palladium nanoparticle pathways
    • C. Rocaboy and J. A. Gladysz, Thermomorphic fluorous imine and thioether palladacycles as precursors for highly active Heck and Suzuki catalysts; evidence for palladium nanoparticle pathways, New. J. Chem., 27, 39-49 (2003).
    • (2003) New. J. Chem. , vol.27 , pp. 39-49
    • Rocaboy, C.1    Gladysz, J.A.2
  • 85
    • 36849096119 scopus 로고    scopus 로고
    • Palladium-catalyzed Heck reaction under thermomorphic mode
    • N. Lu, S. -C. Chen, T. -C. Chen, and L. -K. Liu, Palladium-catalyzed Heck reaction under thermomorphic mode, Tetrahedron Lett., 49, 371-375 (2008).
    • (2008) Tetrahedron Lett. , vol.49 , pp. 371-375
    • Lu, N.1    Chen, S.-C.2    Chen, T.-C.3    Liu, L.-K.4
  • 86
    • 0345097510 scopus 로고    scopus 로고
    • Polymeric phosphine ligand from ring-opening metathesis polymerization of a norbornene derivative. Applications in the Heck, Sonogashira, and Negishi reactions
    • Y. C. Yang and T. Y. Luh, Polymeric phosphine ligand from ring-opening metathesis polymerization of a norbornene derivative. Applications in the Heck, Sonogashira, and Negishi reactions, J. Org. Chem., 68, 9870-9873 (2003).
    • (2003) J. Org. Chem. , vol.68 , pp. 9870-9873
    • Yang, Y.C.1    Luh, T.Y.2
  • 87
    • 39149085338 scopus 로고    scopus 로고
    • A cycloalkane-based thermomorphic system for palladium-catalyzed cross-coupling reactions
    • S. Kim, K. Yamamoto, K. Hayashi, and K. Chiba, A cycloalkane-based thermomorphic system for palladium-catalyzed cross-coupling reactions, Tetrahedron, 64, 2855-2863 (2008).
    • (2008) Tetrahedron , vol.64 , pp. 2855-2863
    • Kim, S.1    Yamamoto, K.2    Hayashi, K.3    Chiba, K.4
  • 88
    • 0037451416 scopus 로고    scopus 로고
    • Homogeneous catalysts supported on soluble polymers: Biphasic Sonogashira coupling of aryl halides and acetylenes using MeOPEG-bound phosphine-palladium catalysts for efficient catalyst recycling
    • A. Kollhofer and H. Plenio, Homogeneous catalysts supported on soluble polymers: Biphasic Sonogashira coupling of aryl halides and acetylenes using MeOPEG-bound phosphine-palladium catalysts for efficient catalyst recycling, Chem. Eur. J., 9, 1416-1425 (2003).
    • (2003) Chem. Eur. J , vol.9 , pp. 1416-1425
    • Kollhofer, A.1    Plenio, H.2
  • 89
    • 0348140969 scopus 로고    scopus 로고
    • Continuous biphasic catalysis: palladium catalyzed cross coupling reactions
    • J. Hillerich and H. Plenio, Continuous biphasic catalysis: palladium catalyzed cross coupling reactions, Chem. Commun., 3024-3025 (2003).
    • (2003) Chem. Commun. , pp. 3024-3025
    • Hillerich, J.1    Plenio, H.2
  • 90
    • 0037804586 scopus 로고    scopus 로고
    • Nonpolar biphasic catalysis: Sonogashira and Suzuki coupling of aryl bromides and chlorides
    • A. Datta and H. Plenio, Nonpolar biphasic catalysis: Sonogashira and Suzuki coupling of aryl bromides and chlorides, Chem. Commun., 1504-1505 (2003).
    • (2003) Chem. Commun. , pp. 1504-1505
    • Datta, A.1    Plenio, H.2
  • 91
    • 0142008869 scopus 로고    scopus 로고
    • Recyclable catalyst with cationic phase tags for the Sonogashira coupling of aryl bromides and aryl chlorides
    • H. Remmele, A. Koelhofer, and H. Plenio, Recyclable catalyst with cationic phase tags for the Sonogashira coupling of aryl bromides and aryl chlorides, Organometallics, 22, 4098-4103 (2003).
    • (2003) Organometallics , vol.22 , pp. 4098-4103
    • Remmele, H.1    Koelhofer, A.2    Plenio, H.3
  • 92
    • 1842733481 scopus 로고    scopus 로고
    • Homogeneous catalysts supported on soluble polymers: biphasic Suzuki-Miyaura coupling of aryl chlorides using phase-tagged palladium-phosphine catalysts
    • M. an der Heiden and H. Plenio, Homogeneous catalysts supported on soluble polymers: biphasic Suzuki-Miyaura coupling of aryl chlorides using phase-tagged palladium-phosphine catalysts, Chem. Eur. J., 10, 1789-1797 (2004).
    • (2004) Chem. Eur. J. , vol.10 , pp. 1789-1797
    • An Der Heiden, M.1    Plenio, H.2
  • 93
    • 43149097364 scopus 로고    scopus 로고
    • Aqueous/organic cross coupling: sustainable protocol for Sonogashira reactions of heterocycles
    • C. A. Fleckenstein and H. Plenio, Aqueous/organic cross coupling: sustainable protocol for Sonogashira reactions of heterocycles, Green Chem., 10, 563-570 (2008).
    • (2008) Green Chem. , vol.10 , pp. 563-570
    • Fleckenstein, C.A.1    Plenio, H.2
  • 94
    • 42149178747 scopus 로고    scopus 로고
    • Efficient Suzuki-Miyaura coupling of (hetero)aryl chlorides with thiophene-and furanboronic acids in aqueous n-butanol
    • C. A. Fleckenstein and H. Plenio, Efficient Suzuki-Miyaura coupling of (hetero)aryl chlorides with thiophene-and furanboronic acids in aqueous n-butanol, J. Org. Chem., 73, 3236-3244 (2008).
    • (2008) J. Org. Chem. , vol.73 , pp. 3236-3244
    • Fleckenstein, C.A.1    Plenio, H.2
  • 95
    • 4143132106 scopus 로고
    • Mutual solubilities of liquids in a binary two-phase system. A physical chemistry experiment
    • A. M. Halpern and S. Gozashti, Mutual solubilities of liquids in a binary two-phase system. A physical chemistry experiment, J. Chem. Educ., 65, 371-372 (1988).
    • (1988) J. Chem. Educ. , vol.65 , pp. 371-372
    • Halpern, A.M.1    Gozashti, S.2
  • 96
    • 30344443388 scopus 로고    scopus 로고
    • Palladium colloid stabilized by block copolymer micelles as an efficient catalyst for reactions of C-C and C-heteroatom bond formation
    • I. P. Beletskaya, A. N. Kashin, A. E. Litvinov, V. S. Tyurin, P. M. Valetsky, and G. van Koten, Palladium colloid stabilized by block copolymer micelles as an efficient catalyst for reactions of C-C and C-heteroatom bond formation, Organometallics, 25, 154-158 (2006).
    • (2006) Organometallics , vol.25 , pp. 154-158
    • Beletskaya, I.P.1    Kashin, A.N.2    Litvinov, A.E.3    Tyurin, V.S.4    Valetsky, P.M.5    Van Koten, G.6
  • 97
    • 34447107134 scopus 로고    scopus 로고
    • 'Green' atom transfer radical polymerization: from process design to Preparation of well-defined environmentally friendly polymeric materials
    • N. V. Tsarevsky and K. Matyjaszewski, 'Green' atom transfer radical polymerization: from process design to Preparation of well-defined environmentally friendly polymeric materials, Chem. Rev., 107, 2270-2299 (2007).
    • (2007) Chem. Rev. , vol.107 , pp. 2270-2299
    • Tsarevsky, N.V.1    Matyjaszewski, K.2
  • 98
    • 0033690709 scopus 로고    scopus 로고
    • Atom transfer radical polymerization of methyl methacrylate with polyethylene-functionalized ligands
    • S. Liou, J. T. Rademacher, D. Malaba, M. E. Pallack, and W. J. Brittain, Atom transfer radical polymerization of methyl methacrylate with polyethylene-functionalized ligands, Macromolecules, 33, 4295-4296 (2000).
    • (2000) Macromolecules , vol.33 , pp. 4295-4296
    • Liou, S.1    Rademacher, J.T.2    Malaba, D.3    Pallack, M.E.4    Brittain, W.J.5
  • 99
    • 0035826989 scopus 로고    scopus 로고
    • Soluble and recoverable support for copper bromide-mediated living radical polymerization
    • Y. Shen, S. Zhu, and R. Pelton, Soluble and recoverable support for copper bromide-mediated living radical polymerization, Macromolecules, 34, 3182-3185 (2001).
    • (2001) Macromolecules , vol.34 , pp. 3182-3185
    • Shen, Y.1    Zhu, S.2    Pelton, R.3
  • 100
    • 3042685966 scopus 로고    scopus 로고
    • Closer to the 'ideal recoverable catalyst' for atom transfer radical polymerization using a molecular non-fluorous thermomorphic system
    • Barre, D. Taton, D Lastecoueres, and J. -M. Vincent Closer to the 'ideal recoverable catalyst' for atom transfer radical polymerization using a molecular non-fluorous thermomorphic system, J. Am. Chem. Soc., 126, 7764-7765 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 7764-7765
    • Taton, B.D.1    Lastecoueres, D.2    Vincent, J.-M.3
  • 101
    • 35949003176 scopus 로고    scopus 로고
    • Self-separating homogeneous copper(I) catalysts
    • D. E. Bergbreiter, P. N. Hamilton, and N. M. Koshti, Self-separating homogeneous copper(I) catalysts, J. Am. Chem. Soc., 109, 10666-10667 (2008).
    • (2008) J. Am. Chem. Soc. , vol.109 , pp. 10666-10667
    • Bergbreiter, D.E.1    Hamilton, P.N.2    Koshti, N.M.3
  • 102
    • 56749155536 scopus 로고    scopus 로고
    • New fluorous bipyridine ligands for copper-catalyzed atom transfer radical polymerization of methyl methacrylate in the thermomorphic mode
    • N. Lu, C. -L. Lin, and T. -C. Chen, New fluorous bipyridine ligands for copper-catalyzed atom transfer radical polymerization of methyl methacrylate in the thermomorphic mode, J. Appl. Polym. Sci., 110, 2531-2537 (2008).
    • (2008) J. Appl. Polym. Sci. , vol.110 , pp. 2531-2537
    • Lu, N.1    Lin, C.-L.2    Chen, T.-C.3
  • 104
    • 0035929950 scopus 로고    scopus 로고
    • Fluorous catalysis without fluorous solvents: a friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid phase separation
    • M. Wende, R. Meier, and J. A. Gladysz, Fluorous catalysis without fluorous solvents: a friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid phase separation, J. Am. Chem. Soc, 123, 11490-11491 (2001).
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 11490-11491
    • Wende, M.1    Meier, R.2    Gladysz, J.A.3
  • 105
    • 0037955542 scopus 로고    scopus 로고
    • Fluorous catalysis under homogeneous conditions without fluorous solvents: a 'greener' catalyst recycling protocol based upon temperature-dependent solubilities and liquid/solid phase separation
    • M. Wende and J. A. Gladysz, Fluorous catalysis under homogeneous conditions without fluorous solvents: a 'greener' catalyst recycling protocol based upon temperature-dependent solubilities and liquid/solid phase separation, J. Am. Chem. Soc., 125, 5861-5872 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 5861-5872
    • Wende, M.1    Gladysz, J.A.2
  • 106
    • 21244462784 scopus 로고    scopus 로고
    • 'Catalyst-on-a-tape'-Teflon: A new delivery and recovery method for homogeneous fluorous catalysts
    • L. V. Dinh and J. A. Gladysz, 'Catalyst-on-a-tape'-Teflon: A new delivery and recovery method for homogeneous fluorous catalysts, Angew. Chem., Int. Ed., 44, 4095-4097 (2005).
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 4095-4097
    • Dinh, L.V.1    Gladysz, J.A.2
  • 107
    • 55049098255 scopus 로고    scopus 로고
    • Catalysis of intramolecular Morita-Baylis-Hillman and Rauhut-Currier reactions by fluorous phosphines; facile recovery by liquid/solid organic/fluorous biphase protocols involving precipitation, Teflon tape, and Gore-Rastex fiber
    • F. O. Seidel and J. A. Gladysz, Catalysis of intramolecular Morita-Baylis-Hillman and Rauhut-Currier reactions by fluorous phosphines; facile recovery by liquid/solid organic/fluorous biphase protocols involving precipitation, Teflon tape, and Gore-Rastex fiber, Adv. Synth. Catal., 350, 2443-2449 (2008).
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2443-2449
    • Seidel, F.O.1    Gladysz, J.A.2
  • 108
    • 33646940976 scopus 로고    scopus 로고
    • Liquid/liquid separation of polysiloxanesupported catalysts
    • M. A. Grunlan, K. R. Regan, and D. E. Bergbreiter, Liquid/liquid separation of polysiloxanesupported catalysts, Chem. Commun., 1715-1717 (2006).
    • (2006) Chem. Commun. , pp. 1715-1717
    • Grunlan, M.A.1    Regan, K.R.2    Bergbreiter, D.E.3
  • 109
    • 15944368537 scopus 로고    scopus 로고
    • Phase selectively soluble dendritic derivative of 4-(N, N-dimethylamino)pyridine: an easily recyclable catalyst for Baylis-Hillman reactions
    • N. F. Yang, H. Gong, W. J. Tang, Q. H. Fan, C. Q. Cai, and L. W. Yang, Phase selectively soluble dendritic derivative of 4-(N, N-dimethylamino)pyridine: an easily recyclable catalyst for Baylis-Hillman reactions, J. Mol. Cat., A: Chem., 233, 55-59 (2005).
    • (2005) J. Mol. Cat., A: Chem. , vol.233 , pp. 55-59
    • Yang, N.F.1    Gong, H.2    Tang, W.J.3    Fan, Q.H.4    Cai, C.Q.5    Yang, L.W.6
  • 110
    • 54549120365 scopus 로고    scopus 로고
    • Ionic transformations in extremely nonpolar fluorous media: easily recoverable phase-transfer catalysts for halide-substitution reactions
    • D. Mandel, M. Jurisch, C. S. M. Consorti, and J. A. Gladysz, Ionic transformations in extremely nonpolar fluorous media: easily recoverable phase-transfer catalysts for halide-substitution reactions, Chem. Asian J., 3, 1772-1782 (2008).
    • (2008) Chem. Asian J. , vol.3 , pp. 1772-1782
    • Mandel, D.1    Jurisch, M.2    Consorti, C.S.M.3    Gladysz, J.A.4
  • 111
    • 38649105770 scopus 로고    scopus 로고
    • A highly active and reusable copper(I)-tren catalyst for the 'click' 1, 3-dipolar cycloaddition of azides and alkynes
    • N. Candelon, D. Lastecoueres, A. K. Diallo, J. Ruiz Aranzaes, D. Astruc, and J. -M. Vincent, A highly active and reusable copper(I)-tren catalyst for the 'click' 1, 3-dipolar cycloaddition of azides and alkynes, Chem. Commun., 741-742 (2008).
    • (2008) Chem. Commun. , pp. 741-742
    • Candelon, N.1    Lastecoueres, D.2    Diallo, A.K.3    Ruiz Aranzaes, J.4    Astruc, D.5    Vincent, J.-M.6
  • 112
    • 13244253633 scopus 로고    scopus 로고
    • Monophasic and biphasic hydrosilylations of enones and ketones using a fluorous rhodium catalyst that is easily recycled under fluorous-organic liquid-liquid biphasic conditions
    • V. L. Dinh and J. A. Gladysz, Monophasic and biphasic hydrosilylations of enones and ketones using a fluorous rhodium catalyst that is easily recycled under fluorous-organic liquid-liquid biphasic conditions, New. J. Chem., 29, 173-181 (2005).
    • (2005) New. J. Chem. , vol.29 , pp. 173-181
    • Dinh, V.L.1    Gladysz, J.A.2
  • 113
    • 31144457771 scopus 로고    scopus 로고
    • Fluorocarbon soluble copper(II) carboxylate complexes with nonfluoroponytailed nitrogen ligands as precatalysts for the oxidation of alkenols and alcohols under fluorous biphasic or thermomorphic modes: structural and mechanistic aspects
    • M. Contel, P. R. Villuendas, J. Fernandez-Gallardo, P. J. Alonso, J. -M. Vincent, and R. H. Fish, Fluorocarbon soluble copper(II) carboxylate complexes with nonfluoroponytailed nitrogen ligands as precatalysts for the oxidation of alkenols and alcohols under fluorous biphasic or thermomorphic modes: structural and mechanistic aspects, Inorg. Chem., 44, 9771-9778 (2005).
    • (2005) Inorg. Chem. , vol.44 , pp. 9771-9778
    • Contel, M.1    Villuendas, P.R.2    Fernandez-Gallardo, J.3    Alonso, P.J.4    Vincent, J.-M.5    Fish, R.H.6
  • 114
    • 36048929232 scopus 로고    scopus 로고
    • Efficient, recoverable, copper-catalyzed aerobic oxidation of alcohols under FBS and thermomorphic mode
    • N. Lu and Y. -C. Lin, Efficient, recoverable, copper-catalyzed aerobic oxidation of alcohols under FBS and thermomorphic mode, Tetrahedron Lett., 48, 8823-8828 (2007).
    • (2007) Tetrahedron Lett. , vol.48 , pp. 8823-8828
    • Lu, N.1    Lin, Y.-C.2
  • 116
    • 50249117652 scopus 로고    scopus 로고
    • Multiphase catalysis in industry
    • H. Hugl and M. Nobis, Multiphase catalysis in industry, Top. Organometal. Chem., 23, 1-17 (2008).
    • (2008) Top. Organometal. Chem. , vol.23 , pp. 1-17
    • Hugl, H.1    Nobis, M.2


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