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Volumn 59, Issue 1-2, 2007, Pages 155-165

Synthesis and photophysical behavior of thia-aza macrocycles with 9-anthracenylmethyl moiety as fluorescent appendage

Author keywords

Extraction; Fluorescence enhancement; OR gate; Sensor; Supramolecular; Synthesis; Thia aza macrocycles

Indexed keywords


EID: 34548690081     PISSN: 09230750     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10847-007-9308-1     Document Type: Article
Times cited : (4)

References (59)
  • 1
    • 37049076125 scopus 로고
    • Metal-ion recognition. Donor-set control of silver(I)/lead(II) discrimination using mixed-donor macrocyclic ligands
    • (a) Adam, K.R., Baldwin, D.S., Bashall, A., Lindoy, L.F., McPartlin, M., Powell, H.R.: Metal-ion recognition. Donor-set control of silver(I)/lead(II) discrimination using mixed-donor macrocyclic ligands. J. Chem. Soc., Dalton Trans. 237-238 (1994)
    • (1994) J. Chem. Soc., Dalton Trans , vol.237-238
    • Adam, K.R.1    Baldwin, D.S.2    Bashall, A.3    Lindoy, L.F.4    McPartlin, M.5    Powell, H.R.6
  • 2
    • 37049084846 scopus 로고
    • Macrocyclic ligand design. Effect of donor-set and ring size variation on silver(I)/lead(II) discrimination within an extended series of dibenzo substituted rings
    • (b) Adam, K.R., Baldwin, D.S., Duckworth, P.A., Lindoy, L.F., McPartlin, M., Bashall, A., Powell, H.R., Tasker, P.A.: Macrocyclic ligand design. Effect of donor-set and ring size variation on silver(I)/lead(II) discrimination within an extended series of dibenzo substituted rings. J. Chem. Soc., Dalton Trans. 1127-1132 (1995)
    • (1995) J. Chem. Soc., Dalton Trans , pp. 1127-1132
    • Adam, K.R.1    Baldwin, D.S.2    Duckworth, P.A.3    Lindoy, L.F.4    McPartlin, M.5    Bashall, A.6    Powell, H.R.7    Tasker, P.A.8
  • 4
    • 0000842021 scopus 로고
    • Tumour targeting with radiolabelled macrocycle-antibody conjugates
    • (a) Parker, D.: Tumour targeting with radiolabelled macrocycle-antibody conjugates. Chem. Soc. Rev. 19, 271-292 (1990)
    • (1990) Chem. Soc. Rev , vol.19 , pp. 271-292
    • Parker, D.1
  • 5
    • 0000916717 scopus 로고    scopus 로고
    • Structural Ion Selectivity of Thia Crown Ether Compounds with a Bulky Block Subunit and Their Application as an Ion-Sensing Component for an Ion-Selective Electrode
    • (b) Siswanta, D., Nagatsuka, K., Yamada, H., Kumakura, K., Hisamoto, H., Shichi, Y., Toshima, K., Suzuki, K.: Structural Ion Selectivity of Thia Crown Ether Compounds with a Bulky Block Subunit and Their Application as an Ion-Sensing Component for an Ion-Selective Electrode. Anal. Chem. 68, 4166-4172 (1996)
    • (1996) Anal. Chem , vol.68 , pp. 4166-4172
    • Siswanta, D.1    Nagatsuka, K.2    Yamada, H.3    Kumakura, K.4    Hisamoto, H.5    Shichi, Y.6    Toshima, K.7    Suzuki, K.8
  • 6
    • 34548698608 scopus 로고
    • A calorimetric titration study of uni-and bivalent metal ion interaction with several thia derivatives of 9-crown-3, 12-crown-4, 15-crown-5, 18-crown-6, 24-crown-8, and with several oxathiapentadecanes in water or water-methanol solvents at 25°C Inorg
    • (a) Izatt, R.M., Terry, R.E., Hansen, L.D., Avondet, A.G., Bradshaw, J.S., Dalley, N.K., Jensen, T.E., Christensen, J.J., Haymore, B.L.: A calorimetric titration study of uni-and bivalent metal ion interaction with several thia derivatives of 9-crown-3, 12-crown-4, 15-crown-5, 18-crown-6, 24-crown-8, and with several oxathiapentadecanes in water or water-methanol solvents at 25°C Inorg. Chim. Acta 30, 1-8, (1978)
    • (1978) Chim. Acta , vol.30 , pp. 1-8
    • Izatt, R.M.1    Terry, R.E.2    Hansen, L.D.3    Avondet, A.G.4    Bradshaw, J.S.5    Dalley, N.K.6    Jensen, T.E.7    Christensen, J.J.8    Haymore, B.L.9
  • 7
    • 33847800118 scopus 로고    scopus 로고
    • Izatt, R.M., Terry, R.E., Haymore, B.L., Hansen, L.D., Dalley, N.K., Avondet, A.G., Christensen, J.J.: Calorimetric titration study of the interaction of several uni- and bivalent cations with 15-crown-5, 18-crown-6, and two isomers of dicyclohexo-18-crown-6 in aqueous solution at 25.degree.C and .mu. = 0.1. J. Am, Chem. Soc. 98, 7620-7626 (1976)
    • (b) Izatt, R.M., Terry, R.E., Haymore, B.L., Hansen, L.D., Dalley, N.K., Avondet, A.G., Christensen, J.J.: Calorimetric titration study of the interaction of several uni- and bivalent cations with 15-crown-5, 18-crown-6, and two isomers of dicyclohexo-18-crown-6 in aqueous solution at 25.degree.C and .mu. = 0.1. J. Am, Chem. Soc. 98, 7620-7626 (1976)
  • 12
    • 33751552840 scopus 로고
    • Ligand design for complexation in aqueous solution. 2. Chelate ring size as a basis for control of size-based selectivity for metal ions
    • (c) Hancock, R.D., Wade, P.W., Ngwenya, M.P., Desousa, A.S., Damu, K.V.: Ligand design for complexation in aqueous solution. 2. Chelate ring size as a basis for control of size-based selectivity for metal ions. Inorg. Chem. 29, 1968-1974 (1990)
    • (1990) Inorg. Chem , vol.29 , pp. 1968-1974
    • Hancock, R.D.1    Wade, P.W.2    Ngwenya, M.P.3    Desousa, A.S.4    Damu, K.V.5
  • 13
    • 33845376023 scopus 로고
    • Coordination of lanthanides by two polyamino polycarboxylic macrocycles: Formation of highly stable lanthanide complexes
    • (d) Lomicin, M.F., Desreux, J.F., Mercing, E.: Coordination of lanthanides by two polyamino polycarboxylic macrocycles: formation of highly stable lanthanide complexes. Inorg. Chem. 25, 2646-2648 (1986)
    • (1986) Inorg. Chem , vol.25 , pp. 2646-2648
    • Lomicin, M.F.1    Desreux, J.F.2    Mercing, E.3
  • 14
    • 33847804075 scopus 로고
    • The synthesis and ion bindings of synthetic multidentate macrocyclic compounds
    • (a) Christensen, J.J., Eatough, D.J., Izatt, R.M.: The synthesis and ion bindings of synthetic multidentate macrocyclic compounds. Chem. Rev. 74, 351-384 (1974)
    • (1974) Chem. Rev , vol.74 , pp. 351-384
    • Christensen, J.J.1    Eatough, D.J.2    Izatt, R.M.3
  • 15
    • 32644459370 scopus 로고
    • Stability constants of cyclic polyether complexes with univalent cations
    • (b) Frensdrof, H.H.: Stability constants of cyclic polyether complexes with univalent cations. J. Am. Chem. Soc. 93, 600-606 (1971)
    • (1971) J. Am. Chem. Soc , vol.93 , pp. 600-606
    • Frensdrof, H.H.1
  • 17
    • 0000694004 scopus 로고
    • Side arm effects on cation binding, extraction, and transport functions of oligopyridine-functionalized aza-crown ethers
    • (b) Tsukube, H.,Uenishi, J., Higaki, H., Kikkawa, K., Tanaka, T., Wakabayashi, S., Oae, S.: Side arm effects on cation binding, extraction, and transport functions of oligopyridine-functionalized aza-crown ethers. J. Org. Chem. 58, 4389-4397 (1993)
    • (1993) J. Org. Chem , vol.58 , pp. 4389-4397
    • Tsukube, H.1    Uenishi, J.2    Higaki, H.3    Kikkawa, K.4    Tanaka, T.5    Wakabayashi, S.6    Oae, S.7
  • 18
    • 0036013814 scopus 로고    scopus 로고
    • Macrocyclic ligand design. Structure-function relationships involving the interaction of pyridinyl-containing, mixed oxygen-nitrogen donor macrocycles with cobalt(II), nickel(II), copper(II), zinc(II), cadmium(II), silver(I) and lead(II)
    • (a) Fenton, R.R., Ganci, R., Junk, P.C., Lindoy, L.F., Lukay, R.C., Meehan, G.V., Prince, J.R., Turner, P., Wei, G.: Macrocyclic ligand design. Structure-function relationships involving the interaction of pyridinyl-containing, mixed oxygen-nitrogen donor macrocycles with cobalt(II), nickel(II), copper(II), zinc(II), cadmium(II), silver(I) and lead(II). J. Chem. Soc., Dalton Trans. 2185-2193 (2002)
    • (2002) J. Chem. Soc., Dalton Trans , pp. 2185-2193
    • Fenton, R.R.1    Ganci, R.2    Junk, P.C.3    Lindoy, L.F.4    Lukay, R.C.5    Meehan, G.V.6    Prince, J.R.7    Turner, P.8    Wei, G.9
  • 19
    • 14244250805 scopus 로고    scopus 로고
    • Novel dithioether-silver(I) coordination architectures: Structural diversities by varying the spacers and terminal groups of ligands
    • (b) Li, J.-R., Bu, X.-H., Du, W.-P., Xu, X.-H., Zhang, R.H.: Novel dithioether-silver(I) coordination architectures: structural diversities by varying the spacers and terminal groups of ligands. J. Chem. Soc., Dalton Trans. 464-474 (2005)
    • (2005) J. Chem. Soc., Dalton Trans , pp. 464-474
    • Li, J.-R.1    Bu, X.-H.2    Du, W.-P.3    Xu, X.-H.4    Zhang, R.H.5
  • 20
    • 22944481804 scopus 로고    scopus 로고
    • About the use of an amide group as a linker in fluoroionophores: Competition between linker and ionophore acting as chelating groups
    • (c) Maton, L., Taziaux, D., Soumillion, J.-P., Jiwan, J.-I.H.: About the use of an amide group as a linker in fluoroionophores: competition between linker and ionophore acting as chelating groups. J. Mater. Chem. 15, 2928-2937 (2005)
    • (2005) J. Mater. Chem , vol.15 , pp. 2928-2937
    • Maton, L.1    Taziaux, D.2    Soumillion, J.-P.3    Jiwan, J.-I.H.4
  • 21
    • 15344340686 scopus 로고    scopus 로고
    • Synthesis and helical polymeric structure of a luminescent pendant-armed macrocyclic silver(I) complex with Ag-Ag interactions
    • (d) Valencia, L.,Bastida, R., Macias, A., Vicente, M., Parez-Lourido, P.: Synthesis and helical polymeric structure of a luminescent pendant-armed macrocyclic silver(I) complex with Ag-Ag interactions. New J. Chem. 29, 424-426 (2005)
    • (2005) New J. Chem , vol.29 , pp. 424-426
    • Valencia, L.1    Bastida, R.2    Macias, A.3    Vicente, M.4    Parez-Lourido, P.5
  • 22
    • 1642533619 scopus 로고    scopus 로고
    • Silver(I) affinities of amides: A combined ab initio and experimental study
    • (e) Ng, K.-M., Li, W.-K., Wo, S.-K., Tsang, C.-W., Ma, N.-L.: Silver(I) affinities of amides: a combined ab initio and experimental study. Phys. Chem. Chem. Phys. 6, 144-153 (2004)
    • (2004) Phys. Chem. Chem. Phys , vol.6 , pp. 144-153
    • Ng, K.-M.1    Li, W.-K.2    Wo, S.-K.3    Tsang, C.-W.4    Ma, N.-L.5
  • 23
    • 0000916717 scopus 로고    scopus 로고
    • Structural ion selectivity of thia crown ether compounds with a bulky block subunit and their application as an ion-sensing component for an ion-selective electrode
    • Siswanta, D., Nagatsuka, K., Yamada, H., Kumakura, K., Hisamoto, H., Scichi, Y., Toshima, K., Suzuki, K.: Structural ion selectivity of thia crown ether compounds with a bulky block subunit and their application as an ion-sensing component for an ion-selective electrode. Anal. Chem. 68, 4166-4172 (1996)
    • (1996) Anal. Chem , vol.68 , pp. 4166-4172
    • Siswanta, D.1    Nagatsuka, K.2    Yamada, H.3    Kumakura, K.4    Hisamoto, H.5    Scichi, Y.6    Toshima, K.7    Suzuki, K.8
  • 28
    • 0032554801 scopus 로고    scopus 로고
    • Synthetic ionophores part 19: Synthesis and ionophore character of 2-aminothiophenol based silver selective acyclic and cyclic receptors
    • Kumar, S., Bhalla, V., Singh, H.: Synthetic ionophores part 19: Synthesis and ionophore character of 2-aminothiophenol based silver selective acyclic and cyclic receptors. Tetrahedron 54, 5575-5586 (1998)
    • (1998) Tetrahedron , vol.54 , pp. 5575-5586
    • Kumar, S.1    Bhalla, V.2    Singh, H.3
  • 31
    • 0030000772 scopus 로고    scopus 로고
    • Synthesis and association behaviour of pyridine based 18-membered diamide - diester - thioether macrocycles
    • (a) Kumar, S., Kaur, N., Singh, H.: Synthesis and association behaviour of pyridine based 18-membered diamide - diester - thioether macrocycles. Tetrahedron Lett. 37, 2071-2072 (1996)
    • (1996) Tetrahedron Lett , vol.37 , pp. 2071-2072
    • Kumar, S.1    Kaur, N.2    Singh, H.3
  • 32
    • 0030583529 scopus 로고    scopus 로고
    • + selectivity in 18-membered diamide -diester macrocycles
    • + selectivity in 18-membered diamide -diester macrocycles. Tetrahedron 52, 13483-13492 (1996)
    • (1996) Tetrahedron , vol.52 , pp. 13483-13492
    • Kumar, S.1    Kaur, N.2    Singh, H.3
  • 33
    • 0347768472 scopus 로고    scopus 로고
    • Synthetic ionophores. Part 20: Synthesis and ionophore character of 2-aminothiophenol and 1,3-/1,4-phenylene based silver selective receptors
    • Kumar, S., Kaur, S., Singh, H.: Synthetic ionophores. Part 20: Synthesis and ionophore character of 2-aminothiophenol and 1,3-/1,4-phenylene based silver selective receptors. J. Inclusion Phenom. Macrocycl. Chem. 39, 277-283 (2001)
    • (2001) J. Inclusion Phenom. Macrocycl. Chem , vol.39 , pp. 277-283
    • Kumar, S.1    Kaur, S.2    Singh, H.3
  • 34
    • 0029885730 scopus 로고    scopus 로고
    • Ni(II), Cu(II), and Zn(II) Cryptate-enhanced fluorescence of a trianthrylcryptand: A potential molecular photonic OR operator
    • (a) Ghosh, P., Bharadwaj, P.K., Mandel, S., Ghosh, S.: Ni(II), Cu(II), and Zn(II) Cryptate-enhanced fluorescence of a trianthrylcryptand: A potential molecular photonic OR operator. J. Am. Chem. Soc. 118, 1553-1554 (1996)
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 1553-1554
    • Ghosh, P.1    Bharadwaj, P.K.2    Mandel, S.3    Ghosh, S.4
  • 35
    • 84942719154 scopus 로고
    • Fluorescent signalling crown ethers; 'switching on' of fluorescence by alkali metal ion recognition and binding in situ
    • (b) de Silva, A.P., de Silva, S.A.: Fluorescent signalling crown ethers; 'switching on' of fluorescence by alkali metal ion recognition and binding in situ. J. Chem. Soc., Chem. Commun. 1709-1710 (1986)
    • (1986) J. Chem. Soc., Chem. Commun , vol.1709-1710
    • de Silva, A.P.1    de Silva, S.A.2
  • 36
    • 34548673241 scopus 로고
    • Off-on fluorescent sensors for physiological levels of magnesium ions based on photoinduced electron transfer (PET), which also behave as photoionic OR logic gates
    • (c) de Silva, A.P., Gunnaratne, H.Q.N., Maguire, G.E.M.: Off-on fluorescent sensors for physiological levels of magnesium ions based on photoinduced electron transfer (PET), which also behave as photoionic OR logic gates. J. Chem. Soc., Chem. Commun. 1213-1214 (1994)
    • (1994) J. Chem. Soc., Chem. Commun , vol.1213-1214
    • de Silva, A.P.1    Gunnaratne, H.Q.N.2    Maguire, G.E.M.3
  • 37
    • 0002615376 scopus 로고    scopus 로고
    • Modulation of metal-fiuorophore communication to develop structurally simpler sensors for transition metal ions
    • (a) Ramachandram, B., Samanta, A.: Modulation of metal-fiuorophore communication to develop structurally simpler sensors for transition metal ions. J. Chem. Soc., Chem. Commun. 1037-1038 (1997)
    • (1997) J. Chem. Soc., Chem. Commun , vol.1037-1038
    • Ramachandram, B.1    Samanta, A.2
  • 38
    • 0001117769 scopus 로고    scopus 로고
    • Transition metal ion induced fluorescence enhancement of 4-(N,N-Dimethylethylenediamino)-7-nitrobenz-2-oxa-1, 3-diazole
    • (b) Ramachandram, B., Samanta, A.: Transition metal ion induced fluorescence enhancement of 4-(N,N-Dimethylethylenediamino)-7-nitrobenz-2-oxa-1, 3-diazole. J. Phys. Chem. A. 102, 10579-10587 (1998)
    • (1998) J. Phys. Chem. A , vol.102 , pp. 10579-10587
    • Ramachandram, B.1    Samanta, A.2
  • 39
    • 0000336184 scopus 로고    scopus 로고
    • Unusually high fluorescence enhancement of some1,8-Naphthalimide derivatives induced by transition metal salts
    • (c) Ramachandram, B., Saroja, G., Sankaran, N.B., Samanta, A.: Unusually high fluorescence enhancement of some1,8-Naphthalimide derivatives induced by transition metal salts. J. Phys. Chem. B. 104, 11824-11832 (2000)
    • (2000) J. Phys. Chem. B , vol.104 , pp. 11824-11832
    • Ramachandram, B.1    Saroja, G.2    Sankaran, N.B.3    Samanta, A.4
  • 41
    • 0035983127 scopus 로고    scopus 로고
    • Rigidization, preorientation and electronic decoupling - the 'magic triangle' for the design of highly efficient fluorescent sensors and switches
    • (b) Rurack, K., Resch-Genger, U.: Rigidization, preorientation and electronic decoupling - the 'magic triangle' for the design of highly efficient fluorescent sensors and switches. Chem. Soc. Rev. 31, 116-127 (2002)
    • (2002) Chem. Soc. Rev , vol.31 , pp. 116-127
    • Rurack, K.1    Resch-Genger, U.2
  • 43
    • 0035801512 scopus 로고    scopus 로고
    • Sensing a paradigm shift in the field of molecular recognition: From selective to differential receptors
    • (d) Lavigne, J.J., Anslyn, E.V.: Sensing a paradigm shift in the field of molecular recognition: From selective to differential receptors. Angew. Chem. Int. Ed. 40, 3118-3130 (2001)
    • (2001) Angew. Chem. Int. Ed , vol.40 , pp. 3118-3130
    • Lavigne, J.J.1    Anslyn, E.V.2
  • 44
    • 0033826120 scopus 로고    scopus 로고
    • The design of luminescent sensors for anions and ionisable analytes
    • (e) Fabbrizzi, L., Licchelli, M., Rabaioli, G., Taglietti, A.F.: The design of luminescent sensors for anions and ionisable analytes. Coord. Chem. Rev. 205, 85-108 (2000)
    • (2000) Coord. Chem. Rev , vol.205 , pp. 85-108
    • Fabbrizzi, L.1    Licchelli, M.2    Rabaioli, G.3    Taglietti, A.F.4
  • 45
    • 0033830295 scopus 로고    scopus 로고
    • Combining luminescence, coordination and electron transfer for signalling purposes
    • (f) de Silva, A.P., Fox, D.B., Huxley, A.J.M., Moody, T.S.: Combining luminescence, coordination and electron transfer for signalling purposes. Coord. Chem. Rev. 205, 41-57 (2000)
    • (2000) Coord. Chem. Rev , vol.205 , pp. 41-57
    • de Silva, A.P.1    Fox, D.B.2    Huxley, A.J.M.3    Moody, T.S.4
  • 48
    • 23644444124 scopus 로고    scopus 로고
    • Luminescent sensors and switches in the early 21st century
    • (b) Callan, J.F., de Silva, A.P., Magri, D.C.: Luminescent sensors and switches in the early 21st century. Tetrahedron 61, 8551-8588 (2005)
    • (2005) Tetrahedron , vol.61 , pp. 8551-8588
    • Callan, J.F.1    de Silva, A.P.2    Magri, D.C.3
  • 49
    • 33747415137 scopus 로고    scopus 로고
    • Consolidating molecular AND logic with two chemical inputs
    • (a) Magri, D.C., Coen, G.D., Boyd, R.L., de Silva, A.P.: Consolidating molecular AND logic with two chemical inputs. Anal. Chim, Acta. 568, 156-160 (2006)
    • (2006) Anal. Chim, Acta , vol.568 , pp. 156-160
    • Magri, D.C.1    Coen, G.D.2    Boyd, R.L.3    de Silva, A.P.4
  • 50
    • 33646129929 scopus 로고    scopus 로고
    • Communicating chemical congregation: A molecular AND logic gate with three chemical inputs as a "Lab-on-a-Molecule" prototype
    • (b) Magri, D.C., Brown, G.J., McClean, G.D., de Silva, A.P.: Communicating chemical congregation: A molecular AND logic gate with three chemical inputs as a "Lab-on-a-Molecule" prototype. J. Am. Chem. Soc. 128, 4950-4951 (2006)
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 4950-4951
    • Magri, D.C.1    Brown, G.J.2    McClean, G.D.3    de Silva, A.P.4
  • 51
    • 0015498786 scopus 로고
    • Interactions of transition-metal ions with photoexcited states of flavines. Fluorescence quenching studies
    • Mostly transition metal ions are notorious quenchers of fluorescence, see
    • Mostly transition metal ions are notorious quenchers of fluorescence, see: Varnes, A.W., Dodson, R.B., Wehry, E.L.: Interactions of transition-metal ions with photoexcited states of flavines. Fluorescence quenching studies. J. Am. Chem. Soc. 94, 946-950 (1972).
    • (1972) J. Am. Chem. Soc , vol.94 , pp. 946-950
    • Varnes, A.W.1    Dodson, R.B.2    Wehry, E.L.3
  • 52
    • 0032758939 scopus 로고    scopus 로고
    • Transition metals as switches
    • For reviews on fluorosensors for transition metal ions, see: a
    • For reviews on fluorosensors for transition metal ions, see: (a) Fabbrizzi, L., Licchelli, M., Pallavicini, P.: Transition metals as switches. Acc. Chem. Res. 32, 846-853 (1999)
    • (1999) Acc. Chem. Res , vol.32 , pp. 846-853
    • Fabbrizzi, L.1    Licchelli, M.2    Pallavicini, P.3
  • 54
    • 33751385009 scopus 로고
    • A convenient procedure for bromomethylation of aromatic compounds. Selective mono-, bis-, or trisbromomethylation
    • van der Made, A.W., van der Made, R.H.: A convenient procedure for bromomethylation of aromatic compounds. Selective mono-, bis-, or trisbromomethylation. J. Org. Chem. 58, 1262-1263 (1993)
    • (1993) J. Org. Chem , vol.58 , pp. 1262-1263
    • van der Made, A.W.1    van der Made, R.H.2
  • 55
    • 33947449185 scopus 로고
    • Bis(bromomethyl) compounds
    • Wilhelm, W.: Bis(bromomethyl) compounds. J. Org. Chem. 17, 523-528 (1952)
    • (1952) J. Org. Chem , vol.17 , pp. 523-528
    • Wilhelm, W.1
  • 56
    • 37049081365 scopus 로고
    • Synthetic ionophores. Part 8. Amide-ether-amine-containing macrocycles: Synthesis, transport and binding of metal cations
    • Kumar, S., Singh, R., Singh, H.: Synthetic ionophores. Part 8. Amide-ether-amine-containing macrocycles: synthesis, transport and binding of metal cations. J. Chem. Soc., Perkin Trans. 1, 3049-3054 (1992)
    • (1992) J. Chem. Soc., Perkin Trans. 1 , pp. 3049-3054
    • Kumar, S.1    Singh, R.2    Singh, H.3
  • 57
    • 34548669541 scopus 로고    scopus 로고
    • The energy minimized conformations of receptors 10-13 and 16-19 have been computed by using PM3 calculations available in the CAChe 3.1 software
    • The energy minimized conformations of receptors 10-13 and 16-19 have been computed by using PM3 calculations available in the CAChe 3.1 software
  • 58
    • 0346821278 scopus 로고
    • Host-guest complexation. 4. Remote substituent effects on macrocyclic polyether binding to metal and ammonium ions
    • (a) Moore, S.S., Tarnowski, T.L., Newcomb, M., Cram, D.J.: Host-guest complexation. 4. Remote substituent effects on macrocyclic polyether binding to metal and ammonium ions. J. Am. Chem. Soc. 99, 6398-6405 (1977)
    • (1977) J. Am. Chem. Soc , vol.99 , pp. 6398-6405
    • Moore, S.S.1    Tarnowski, T.L.2    Newcomb, M.3    Cram, D.J.4
  • 59
    • 5344244992 scopus 로고
    • Host-guest complexation. 16. Synthesis and cation binding characteristics of macrocyclic polyethers containing convergent methoxyaryl groups
    • (b) Koeing, K.E., Lehn, J.M., Stuckler, P., Kaneda, T., Cram, D.J.: Host-guest complexation. 16. Synthesis and cation binding characteristics of macrocyclic polyethers containing convergent methoxyaryl groups. J. Am. Chem. Soc. 101, 3553-3566 (1979)
    • (1979) J. Am. Chem. Soc , vol.101 , pp. 3553-3566
    • Koeing, K.E.1    Lehn, J.M.2    Stuckler, P.3    Kaneda, T.4    Cram, D.J.5


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