메뉴 건너뛰기




Volumn 5, Issue 1, 2013, Pages 42-47

Halogen-bonding-triggered supramolecular gel formation

Author keywords

[No Author keywords available]

Indexed keywords

1,4 DIIODOTETRAFLUOROBENZENE; 1,4-DIIODOTETRAFLUOROBENZENE; BENZENE DERIVATIVE; DIMETHYL SULFOXIDE; HALOGEN; HALOGENATED HYDROCARBON; METHANOL; PYRIDINE; PYRIDINE DERIVATIVE; UREA; WATER;

EID: 84871577538     PISSN: 17554330     EISSN: 17554349     Source Type: Journal    
DOI: 10.1038/nchem.1496     Document Type: Article
Times cited : (391)

References (57)
  • 1
    • 84889427047 scopus 로고    scopus 로고
    • eds Atwood, J. L. & Steedin, J. W, Wiley-VCH
    • Smith, D. K. in Organic Nanostructures (eds Atwood, J. L. & Steedin, J. W.) 111-154 (Wiley-VCH, 2008).
    • (2008) Organic Nanostructures , pp. 111-154
    • Smith, D.K.1
  • 2
    • 54049115951 scopus 로고    scopus 로고
    • High-tech applications of self-assembling supramolecular nanostructured gel-phase materials: From regenerative medicine to electronic devices
    • Hirst, A. R., Escuder, B., Miravet, J. F. & Smith, D. K. High-tech applications of self-assembling supramolecular nanostructured gel-phase materials: from regenerative medicine to electronic devices. Angew. Chem. Int. Ed. 47, 8002-8018 (2008).
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8002-8018
    • Hirst, A.R.1    Escuder, B.2    Miravet, J.F.3    Smith, D.K.4
  • 3
    • 78649502831 scopus 로고    scopus 로고
    • Supramolecular gels: Anion-switchable media for controlling crystal growth
    • Foster, J. A. et al. Supramolecular gels: anion-switchable media for controlling crystal growth. Nature Chem. 2, 1037-1043 (2010).
    • (2010) Nature Chem. , vol.2 , pp. 1037-1043
    • Foster, J.A.1
  • 4
    • 79551674013 scopus 로고    scopus 로고
    • Gel incorporation inside of organic single crystals grown in agarose hydrogels
    • Li, H., Fujiki, Y., Sada, K. & Estroff, L. A. Gel incorporation inside of organic single crystals grown in agarose hydrogels. CrystEngComm 13, 1060-1062 (2011).
    • (2011) CrystEngComm , vol.13 , pp. 1060-1062
    • Li, H.1    Fujiki, Y.2    Sada, K.3    Estroff, L.A.4
  • 5
    • 1842454609 scopus 로고    scopus 로고
    • Water gelation by small organic molecules
    • Estroff, L. A. & Hamilton, A. D. Water gelation by small organic molecules. Chem. Rev. 104, 1201-1217 (2004).
    • (2004) Chem. Rev. , vol.104 , pp. 1201-1217
    • Estroff, L.A.1    Hamilton, A.D.2
  • 6
    • 1642420635 scopus 로고    scopus 로고
    • An organic hydrogel as a matrix for the growth of calcite crystals
    • Estroff, L. A., Addadi, L.,Weiner, S. & Hamilton, A. D. An organic hydrogel as a matrix for the growth of calcite crystals. Org. Biomol. Chem. 2, 137-141 (2004).
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 137-141
    • Estroff, L.A.1    Addadi, L.2    Weiner, S.3    Hamilton, A.D.4
  • 8
    • 25444531477 scopus 로고    scopus 로고
    • Self-assembly of small molecules affords multifunctional supramolecular hydrogels for topically treating simulated uranium wounds
    • Yang, Z. et al. Self-assembly of small molecules affords multifunctional supramolecular hydrogels for topically treating simulated uranium wounds. Chem. Commun. 4414-4416 (2005).
    • (2005) Chem. Commun. , pp. 4414-4416
    • Yang, Z.1
  • 9
    • 77953155679 scopus 로고    scopus 로고
    • Supramolecular gels as active media for organic reactions and catalysis
    • Escuder, B., Rodríguez-Llansola, F. & Miravet, J. F. Supramolecular gels as active media for organic reactions and catalysis. New J. Chem. 34, 1044-1054 (2010).
    • (2010) New J. Chem. , vol.34 , pp. 1044-1054
    • Escuder, B.1    Rodríguez-Llansola, F.2    Miravet, J.F.3
  • 10
    • 0001629673 scopus 로고    scopus 로고
    • Low molecular mass gelators of organic liquids and the properties of their gels
    • Terech, P. &Weiss, R. G. Low molecular mass gelators of organic liquids and the properties of their gels. Chem. Rev. 97, 3133-3160 (1997).
    • (1997) Chem. Rev. , vol.97 , pp. 3133-3160
    • Terech, P.1    Weiss, R.G.2
  • 11
    • 56549113108 scopus 로고    scopus 로고
    • Supramolecular gelling agents: Can they be designed?
    • Dastidar, P. Supramolecular gelling agents: can they be designed? Chem. Soc. Rev. 37, 2699-2715 (2008).
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 2699-2715
    • Dastidar, P.1
  • 12
    • 33746297079 scopus 로고    scopus 로고
    • Metal coordination to assist molecular gelation
    • Fages, F. Metal coordination to assist molecular gelation. Angew. Chem. Int. Ed. 45, 1680-1682 (2006).
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1680-1682
    • Fages, F.1
  • 13
    • 77956580785 scopus 로고    scopus 로고
    • Exploiting cavities in supramolecular gels
    • Foster, J. A. & Steed, J. W. Exploiting cavities in supramolecular gels. Angew. Chem. Int. Ed. 49, 6718-6724 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 6718-6724
    • Foster, J.A.1    Steed, J.W.2
  • 14
    • 57649156256 scopus 로고    scopus 로고
    • Anion-responsive supramolecular gels
    • Maeda, H. Anion-responsive supramolecular gels. Chem. Eur. J. 14, 11274-11282 (2008).
    • (2008) Chem. Eur. J. , vol.14 , pp. 11274-11282
    • Maeda, H.1
  • 15
    • 78751557975 scopus 로고    scopus 로고
    • Supramolecular gel chemistry: Developments over the last decade
    • Steed, J. W. Supramolecular gel chemistry: developments over the last decade. Chem. Commun. 47, 1379-1383 (2011).
    • (2011) Chem. Commun. , vol.47 , pp. 1379-1383
    • Steed, J.W.1
  • 16
    • 68849118037 scopus 로고    scopus 로고
    • Switchable perfomance of an l-proline-derived basic catalyst controlled by supramolecular gelation
    • Rodríguez-Llansola, F., Escuder, B. & Miravet, J. F. Switchable perfomance of an l-proline-derived basic catalyst controlled by supramolecular gelation. J. Am. Chem. Soc. 131, 11478-11484 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 11478-11484
    • Rodríguez-Llansola, F.1    Escuder, B.2    Miravet, J.F.3
  • 17
    • 34547374564 scopus 로고    scopus 로고
    • Switchable fluorescent organogels and mesomorphic superstructure based on naphthalene derivatives
    • Yang, H. et al. Switchable fluorescent organogels and mesomorphic superstructure based on naphthalene derivatives. Langmuir 23, 8224-8230 (2007).
    • (2007) Langmuir , vol.23 , pp. 8224-8230
    • Yang, H.1
  • 18
    • 78649627683 scopus 로고    scopus 로고
    • Acid/base-and anion-controllable organogels formed from a urea-based molecular switch
    • Hsueh, S-Y. et al. Acid/base- and anion-controllable organogels formed from a urea-based molecular switch. Angew. Chem. Int. Ed. 49, 9170-9173 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9170-9173
    • Hsueh, S.-Y.1
  • 19
    • 67749113465 scopus 로고    scopus 로고
    • Ultrasound-induced switching of sheetlike coordination polymer microparticles to nanofibers capable of gelating solvents
    • Zhang, S. Y. et al. Ultrasound-induced switching of sheetlike coordination polymer microparticles to nanofibers capable of gelating solvents. J. Am. Chem. Soc. 131, 1689-1691 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 1689-1691
    • Zhang, S.Y.1
  • 20
    • 64549163746 scopus 로고    scopus 로고
    • Counterion dependent hydrogelation of amino acid based amphiphiles: Switching from non-gelators to gelators and facile synthesis of silver nanoparticles
    • Dutta, S., Shome, A., Debnath, S. & Das, P. K. Counterion dependent hydrogelation of amino acid based amphiphiles: switching from non-gelators to gelators and facile synthesis of silver nanoparticles. Soft Matter 5, 1607-1620 (2009).
    • (2009) Soft Matter , vol.5 , pp. 1607-1620
    • Dutta, S.1    Shome, A.2    Debnath, S.3    Das, P.K.4
  • 21
    • 57149120519 scopus 로고    scopus 로고
    • Redox-responsive gel-sol/sol-gel transition in poly(acrylic acid) aqueous solution containing Fe(III) ions switched by light
    • Peng, F., Li, G., Liu, X., Wu, S. & Tong, Z. Redox-responsive gel-sol/sol-gel transition in poly(acrylic acid) aqueous solution containing Fe(III) ions switched by light. J. Am. Chem. Soc. 130, 16166-16167 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 16166-16167
    • Peng, F.1    Li, G.2    Liu, X.3    Wu, S.4    Tong, Z.5
  • 22
    • 70350164730 scopus 로고    scopus 로고
    • Molecular self-assembly and patterning induced by sound waves. The case of gelation
    • Cravotto, G. & Cintas, P. Molecular self-assembly and patterning induced by sound waves. The case of gelation. Chem. Soc. Rev. 38, 2684-2697 (2009).
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2684-2697
    • Cravotto, G.1    Cintas, P.2
  • 23
    • 21644446978 scopus 로고    scopus 로고
    • Molecules that assemble by sound: An application to the instant gelation of stable organic fluids
    • Naota, T. & Koori, H. Molecules that assemble by sound: an application to the instant gelation of stable organic fluids. J. Am. Chem. Soc. 127, 9324-9325 (2005).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 9324-9325
    • Naota, T.1    Koori, H.2
  • 24
    • 78649267848 scopus 로고    scopus 로고
    • Anion-tuned supramolecular gels: A natural evolution from urea supramolecular chemistry
    • Steed, J. W. Anion-tuned supramolecular gels: a natural evolution from urea supramolecular chemistry. Chem. Soc. Rev. 39, 3686-3699 (2010).
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 3686-3699
    • Steed, J.W.1
  • 26
    • 50249149519 scopus 로고    scopus 로고
    • Proline-functionalised calix [4]arene: An anion-triggered hydrogelator
    • Becker, T. et al. Proline-functionalised calix[4]arene: an anion-triggered hydrogelator. Chem. Commun. 3900-3902 (2008).
    • (2008) Chem. Commun. , pp. 3900-3902
    • Becker, T.1
  • 27
    • 77956333245 scopus 로고    scopus 로고
    • Anion-triggered melamine based self-assembly and hydrogel
    • Shen, J-S., Cai, Q-G., Jiang, Y-B. & Zhang, H-W. Anion-triggered melamine based self-assembly and hydrogel. Chem. Commun. 46, 6786-6788 (2010).
    • (2010) Chem. Commun. , vol.46 , pp. 6786-6788
    • Shen, J.-S.1    Cai, Q.-G.2    Jiang, Y.-B.3    Zhang, H.-W.4
  • 28
    • 69249214105 scopus 로고    scopus 로고
    • Anion-tuning of supramolecular gel properties
    • Lloyd, G. O. & Steed, J. W. Anion-tuning of supramolecular gel properties. Nature Chem. 1, 437-442 (2009).
    • (2009) Nature Chem. , vol.1 , pp. 437-442
    • Lloyd, G.O.1    Steed, J.W.2
  • 29
    • 44849098068 scopus 로고    scopus 로고
    • Gelation is crucially dependent on functional group orientation and may be tuned by anion binding
    • Piepenbrock, M-O. M., Lloyd, G. O., Clarke, N. & Steed, J. W. Gelation is crucially dependent on functional group orientation and may be tuned by anion binding. Chem. Commun. 2644-2646 (2008).
    • (2008) Chem. Commun. , pp. 2644-2646
    • Piepenbrock, M.-O.M.1    Lloyd, G.O.2    Clarke, N.3    Steed, J.W.4
  • 31
    • 79551469142 scopus 로고    scopus 로고
    • Anion tuning and polymer templating in a simple low molecular weight organogelator
    • Piepenbrock, M-O. M., Clarke, N., Foster, J. A. & Steed, J. W. Anion tuning and polymer templating in a simple low molecular weight organogelator. Chem. Commun. 47, 2095-2097 (2011).
    • (2011) Chem. Commun. , vol.47 , pp. 2095-2097
    • Piepenbrock, M.-O.M.1    Clarke, N.2    Foster, J.A.3    Steed, J.W.4
  • 32
    • 77957772027 scopus 로고    scopus 로고
    • Metal-induced gelation in dipyridyl ureas
    • Byrne, P. et al. Metal-induced gelation in dipyridyl ureas. New J. Chem. 34, 2261-2274 (2010).
    • (2010) New J. Chem. , vol.34 , pp. 2261-2274
    • Byrne, P.1
  • 33
    • 77954826103 scopus 로고    scopus 로고
    • Shear-induced gelation in a copper(II) metallogel: New aspects of ion-tunable rheology and gel-reformation by external chemical stimuli
    • Piepenbrock, M-O. M., Clarke, N. & Steed, J. W. Shear-induced gelation in a copper(II) metallogel: new aspects of ion-tunable rheology and gel-reformation by external chemical stimuli. Soft Matter 6, 3541-3547 (2010).
    • (2010) Soft Matter , vol.6 , pp. 3541-3547
    • Piepenbrock, M.-O.M.1    Clarke, N.2    Steed, J.W.3
  • 34
    • 68149091916 scopus 로고    scopus 로고
    • Metal ion and anion based 'tuning' of a supramolecular metallogel
    • Piepenbrock, M-O. M., Clarke, N. & Steed, J. W. Metal ion and anion based 'tuning' of a supramolecular metallogel. Langmuir 25, 8451-8456 (2009).
    • (2009) Langmuir , vol.25 , pp. 8451-8456
    • Piepenbrock, M.-O.M.1    Clarke, N.2    Steed, J.W.3
  • 35
    • 79953860696 scopus 로고    scopus 로고
    • Recent developments in crystal engineering
    • Biradha, K., Su, C-Y. & Vittal, J. J. Recent developments in crystal engineering. Cryst. Growth Des. 11, 875-886 (2011).
    • (2011) Cryst. Growth Des. , vol.11 , pp. 875-886
    • Biradha, K.1    Su, C.-Y.2    Vittal, J.J.3
  • 36
    • 25844464824 scopus 로고    scopus 로고
    • Crystal engineering with hydrogen bonds and halogen bonds
    • Saha, B. K., Nangia, A. & Jaskolski, M. Crystal engineering with hydrogen bonds and halogen bonds. CrystEngComm 7, 355-358 (2005).
    • (2005) CrystEngComm , vol.7 , pp. 355-358
    • Saha, B.K.1    Nangia, A.2    Jaskolski, M.3
  • 39
    • 34547177726 scopus 로고    scopus 로고
    • Highly interpenetrated supramolecular networks supported by N..I halogen bonding
    • Metrangolo, P., Meyer, F., Pilati, T., Proserpio, D. M. & Resnati, G. Highly interpenetrated supramolecular networks supported by N...I halogen bonding. Chem. Eur. J. 13, 5765-5772 (2007).
    • (2007) Chem. Eur. J. , vol.13 , pp. 5765-5772
    • Metrangolo, P.1    Meyer, F.2    Pilati, T.3    Proserpio, D.M.4    Resnati, G.5
  • 40
    • 20444479110 scopus 로고    scopus 로고
    • Halogen bonding based recognition processes: A world parallel to hydrogen bonding
    • Metrangolo, P., Neukirch, H., Pilati, T. & Resnati, G. Halogen bonding based recognition processes: a world parallel to hydrogen bonding. Acc. Chem. Res. 38, 386-395 (2005).
    • (2005) Acc. Chem. Res. , vol.38 , pp. 386-395
    • Metrangolo, P.1    Neukirch, H.2    Pilati, T.3    Resnati, G.4
  • 42
    • 84255177786 scopus 로고    scopus 로고
    • A cocrystal strategy to tune the luminescent properties of stilbene-type organic solid-state materials
    • Yan, D. et al. A cocrystal strategy to tune the luminescent properties of stilbene-type organic solid-state materials. Angew. Chem. Int. Ed. 50, 12483-12486 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 12483-12486
    • Yan, D.1
  • 43
    • 77955809684 scopus 로고    scopus 로고
    • Halogen bonding: A general route in anion recognition and coordination
    • Cavallo, G. et al. Halogen bonding: a general route in anion recognition and coordination. Chem. Soc. Rev. 39, 3772-3783 (2010).
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 3772-3783
    • Cavallo, G.1
  • 44
    • 83055198430 scopus 로고    scopus 로고
    • Avoiding 'synthon crossover' in crystal engineering with halogen bonds and hydrogen bonds
    • Aakeröy, C. B., Chopade, P. D. & Desper, J. Avoiding 'synthon crossover' in crystal engineering with halogen bonds and hydrogen bonds. Cryst. Growth Des. 11, 5333-5336 (2011).
    • (2011) Cryst. Growth Des. , vol.11 , pp. 5333-5336
    • Aakeröy, C.B.1    Chopade, P.D.2    Desper, J.3
  • 45
    • 79953687103 scopus 로고    scopus 로고
    • Facile synthesis and supramolecular chemistry of hydrogen bond/halogen bond-driven multi-tasking tectons
    • Aakeröy, C. B., Chopade, P. D., Ganser, C. & Desper, J. Facile synthesis and supramolecular chemistry of hydrogen bond/halogen bond-driven multi-tasking tectons. Chem. Commun. 47, 4688-4690 (2011).
    • (2011) Chem. Commun. , vol.47 , pp. 4688-4690
    • Aakeröy, C.B.1    Chopade, P.D.2    Ganser, C.3    Desper, J.4
  • 46
    • 80052232617 scopus 로고    scopus 로고
    • Complementary p-p interactions induce multicomponent coassembly into functional fibrils
    • Ryan, D. M., Doran, T. M. & Nilsson, B. L. Complementary p-p interactions induce multicomponent coassembly into functional fibrils. Langmuir 27, 11145-11156 (2011).
    • (2011) Langmuir , vol.27 , pp. 11145-11156
    • Ryan, D.M.1    Doran, T.M.2    Nilsson, B.L.3
  • 47
    • 34250646619 scopus 로고    scopus 로고
    • Composites of N,N′-bis-(pyridyl) urea-dicarboxylic acid as new hydrogelators - A crystal engineering approach
    • Adarsh, N. N., Kumar, D. K. & Dastidar, P. Composites of N,N′-bis-(pyridyl) urea-dicarboxylic acid as new hydrogelators - a crystal engineering approach. Tetrahedron 63, 7386-7396 (2007).
    • (2007) Tetrahedron , vol.63 , pp. 7386-7396
    • Adarsh, N.N.1    Kumar, D.K.2    Dastidar, P.3
  • 48
    • 58149240787 scopus 로고    scopus 로고
    • Controlled self-sorting in the assembly of multi-gelator gels
    • Moffat, J. R. & Smith, D. K. Controlled self-sorting in the assembly of multi-gelator gels. Chem. Commun. 316-318 (2009).
    • (2009) Chem. Commun. , pp. 316-318
    • Moffat, J.R.1    Smith, D.K.2
  • 49
    • 57649207571 scopus 로고    scopus 로고
    • Gradual transition from NH..pyridyl hydrogen bonding to the NH..O tape synthon in pyridyl ureas
    • Byrne, P., Turner, D. R., Lloyd, G. O., Clarke, N. & Steed, J. W. Gradual transition from NH...pyridyl hydrogen bonding to the NH...O tape synthon in pyridyl ureas. Cryst. Growth Des. 8, 3335-3344 (2008).
    • (2008) Cryst. Growth Des. , vol.8 , pp. 3335-3344
    • Byrne, P.1    Turner, D.R.2    Lloyd, G.O.3    Clarke, N.4    Steed, J.W.5
  • 50
    • 33748268478 scopus 로고    scopus 로고
    • Helical or polar guest-dependent z′=1.5 or z′=2 forms of a sterically hindered bis(urea) clathrate
    • Todd, A. M., Anderson, K. M., Byrne, P., Goeta, A. E. & Steed, J. W. Helical or polar guest-dependent z′=1.5 or z′=2 forms of a sterically hindered bis(urea) clathrate. Cryst. Growth Des. 6, 1750-1752 (2006).
    • (2006) Cryst. Growth Des. , vol.6 , pp. 1750-1752
    • Todd, A.M.1    Anderson, K.M.2    Byrne, P.3    Goeta, A.E.4    Steed, J.W.5
  • 51
    • 0029789766 scopus 로고    scopus 로고
    • Novel X-ray method for in situ determination of gelator strand structure: Polymorphism of cholesteryl anthraquinone-2-carboxylate
    • Ostuni, E., Kamaras, P. & Weiss, R. G. Novel X-ray method for in situ determination of gelator strand structure: polymorphism of cholesteryl anthraquinone-2-carboxylate. Angew. Chem. Int. Ed. Engl. 35, 1324-1326 (1996).
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1324-1326
    • Ostuni, E.1    Kamaras, P.2    Weiss, R.G.3
  • 52
    • 19944369098 scopus 로고    scopus 로고
    • Urea and thiourea derivatives as low molecular-mass organogelators
    • George, M., Tan, G., John, V. T. & Weiss, R. G. Urea and thiourea derivatives as low molecular-mass organogelators. Chem. Eur. J. 11, 3243-3254 (2005).
    • (2005) Chem. Eur. J. , vol.11 , pp. 3243-3254
    • George, M.1    Tan, G.2    John, V.T.3    Weiss, R.G.4
  • 53
    • 38849207592 scopus 로고    scopus 로고
    • Structure calculation of an elastic hydrogel from sonication of rigid small molecule components
    • Anderson, K. M. et al. Structure calculation of an elastic hydrogel from sonication of rigid small molecule components. Angew. Chem. Int. Ed. 47, 1058-1062 (2008).
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1058-1062
    • Anderson, K.M.1
  • 54
    • 0037008131 scopus 로고    scopus 로고
    • Thermodynamics of hydrogen bond patterns in supramolecular assemblies of water molecules
    • Henry, M. Thermodynamics of hydrogen bond patterns in supramolecular assemblies of water molecules. ChemPhysChem 3, 607-616 (2002).
    • (2002) ChemPhysChem , vol.3 , pp. 607-616
    • Henry, M.1
  • 55
    • 0037008141 scopus 로고    scopus 로고
    • Nonempirical quantification of molecular interactions in supramolecular assemblies
    • Henry, M. Nonempirical quantification of molecular interactions in supramolecular assemblies. ChemPhysChem 3, 561-569 (2002).
    • (2002) ChemPhysChem , vol.3 , pp. 561-569
    • Henry, M.1
  • 56
    • 0000867567 scopus 로고    scopus 로고
    • Crystal engineering through halogen bonding: Complexes of nitrogen heterocycles with organic iodides
    • Walsh, R. B. et al. Crystal engineering through halogen bonding: complexes of nitrogen heterocycles with organic iodides. Cryst. Growth Des. 1, 165-175 (2001).
    • (2001) Cryst. Growth Des. , vol.1 , pp. 165-175
    • Walsh, R.B.1
  • 57
    • 0037008629 scopus 로고    scopus 로고
    • 2,3,5,6-Tetrafluorophenylnitren-4-yl a quartetground-state nitrene radical
    • Wenk, H. H. & Sander, W. 2,3,5,6-Tetrafluorophenylnitren-4-yl: a quartetground- state nitrene radical. Angew. Chem. Int. Ed. 41, 2742-2745 (2002).
    • (2002) Angew Chem Int Ed , vol.41 , pp. 2742-2745
    • Wenk, H.H.1    Sander, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.