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Volumn 46, Issue 1, 2013, Pages 181-189

Covalent functionalization of graphene with reactive intermediates

Author keywords

[No Author keywords available]

Indexed keywords

BENZOYL PEROXIDE; DIAZONIUM COMPOUND; FREE RADICAL; GRAPHITE; INORGANIC SALT;

EID: 84872723430     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/ar300172h     Document Type: Article
Times cited : (367)

References (94)
  • 3
    • 42749102313 scopus 로고    scopus 로고
    • Interlayer cohesive energy of graphite from thermal desorption of polyaromatic hydrocarbons
    • Zacharia, R.; Ulbricht, H.; Hertel, T. Interlayer cohesive energy of graphite from thermal desorption of polyaromatic hydrocarbons Phys. Rev. B 2004, 69, 155406
    • (2004) Phys. Rev. B , vol.69 , pp. 155406
    • Zacharia, R.1    Ulbricht, H.2    Hertel, T.3
  • 5
    • 33644659711 scopus 로고    scopus 로고
    • Stable aqueous dispersions of graphitic nanoplatelets via the reduction of exfoliated graphite oxide in the presence of poly(sodium 4-styrenesulfonate)
    • Stankovich, S.; Piner, R. D.; Chen, X.; Wu, N.; Nguyen, S. T.; Ruoff, R. S. Stable aqueous dispersions of graphitic nanoplatelets via the reduction of exfoliated graphite oxide in the presence of poly(sodium 4-styrenesulfonate) J. Mater. Chem. 2006, 16, 155-158
    • (2006) J. Mater. Chem. , vol.16 , pp. 155-158
    • Stankovich, S.1    Piner, R.D.2    Chen, X.3    Wu, N.4    Nguyen, S.T.5    Ruoff, R.S.6
  • 6
    • 81255163031 scopus 로고    scopus 로고
    • Recent Advances in the Covalent Modification of Graphene with Polymers
    • Salavagione, H. J.; Martínez, G.; Ellis, G. Recent Advances in the Covalent Modification of Graphene With Polymers Macromol. Rapid Commun. 2011, 32, 1771-1789
    • (2011) Macromol. Rapid Commun. , vol.32 , pp. 1771-1789
    • Salavagione, H.J.1    Martínez, G.2    Ellis, G.3
  • 7
    • 74949085018 scopus 로고    scopus 로고
    • Water-Soluble Graphene Covalently Functionalized by Biocompatible Poly- l -lysine
    • Shan, C.; Yang, H.; Han, D.; Zhang, Q.; Ivaska, A.; Niu, L. Water-Soluble Graphene Covalently Functionalized by Biocompatible Poly- l -lysine Langmuir 2009, 25, 12030-12033
    • (2009) Langmuir , vol.25 , pp. 12030-12033
    • Shan, C.1    Yang, H.2    Han, D.3    Zhang, Q.4    Ivaska, A.5    Niu, L.6
  • 8
    • 82955190404 scopus 로고    scopus 로고
    • Chemistry and physics of a single atomic layer: Strategies and challenges for functionalization of graphene and graphene-based materials
    • Yan, L.; Zheng, Y. B.; Zhao, F.; Li, S.; Gao, X.; Xu, B.; Weiss, P. S.; Zhao, Y. Chemistry and physics of a single atomic layer: strategies and challenges for functionalization of graphene and graphene-based materials Chem. Soc. Rev. 2012, 41
    • (2012) Chem. Soc. Rev. , pp. 41
    • Yan, L.1    Zheng, Y.B.2    Zhao, F.3    Li, S.4    Gao, X.5    Xu, B.6    Weiss, P.S.7    Zhao, Y.8
  • 11
    • 77956963862 scopus 로고    scopus 로고
    • Graphene and Graphene Oxide: Synthesis, Properties, and Applications
    • Zhu, Y.; Murali, S.; Cai, W.; Li, X.; Suk, J. W.; Potts, J. R.; Ruoff, R. S. Graphene and Graphene Oxide: Synthesis, Properties, and Applications Adv. Mater. 2010, 22, 3906-3924
    • (2010) Adv. Mater. , vol.22 , pp. 3906-3924
    • Zhu, Y.1    Murali, S.2    Cai, W.3    Li, X.4    Suk, J.W.5    Potts, J.R.6    Ruoff, R.S.7
  • 13
    • 34047266170 scopus 로고    scopus 로고
    • Unique chemical reactivity of a graphene nanoribbon's zigzag edge
    • Jiang, D.-e.; Sumpter, B. G.; Dai, S. Unique chemical reactivity of a graphene nanoribbon's zigzag edge J. Chem. Phys. 2007, 126, 134701-6
    • (2007) J. Chem. Phys. , vol.126 , pp. 134701-6
    • Jiang, D.-E.1    Sumpter, B.G.2    Dai, S.3
  • 15
    • 79959788241 scopus 로고    scopus 로고
    • Graphene-Based Materials: Synthesis, Characterization, Properties, and Applications
    • Huang, X.; Yin, Z.; Wu, S.; Qi, X.; He, Q.; Zhang, Q.; Yan, Q.; Boey, F.; Zhang, H. Graphene-Based Materials: Synthesis, Characterization, Properties, and Applications Small 2011, 7, 1876-1902
    • (2011) Small , vol.7 , pp. 1876-1902
    • Huang, X.1    Yin, Z.2    Wu, S.3    Qi, X.4    He, Q.5    Zhang, Q.6    Yan, Q.7    Boey, F.8    Zhang, H.9
  • 16
    • 79956078840 scopus 로고    scopus 로고
    • Liquid-phase exfoliation, functionalization and applications of graphene
    • Cui, X.; Zhang, C.; Hao, R.; Hou, Y. Liquid-phase exfoliation, functionalization and applications of graphene Nanoscale 2011, 3, 2118-2126
    • (2011) Nanoscale , vol.3 , pp. 2118-2126
    • Cui, X.1    Zhang, C.2    Hao, R.3    Hou, Y.4
  • 17
    • 77950240993 scopus 로고    scopus 로고
    • Graphene Oxide, Highly Reduced Graphene Oxide, and Graphene: Versatile Building Blocks for Carbon-Based Materials
    • Compton, O. C.; Nguyen, S. T. Graphene Oxide, Highly Reduced Graphene Oxide, and Graphene: Versatile Building Blocks for Carbon-Based Materials Small 2010, 6, 711-723
    • (2010) Small , vol.6 , pp. 711-723
    • Compton, O.C.1    Nguyen, S.T.2
  • 19
    • 79952129835 scopus 로고    scopus 로고
    • Functional Composite Materials Based on Chemically Converted Graphene
    • Bai, H.; Li, C.; Shi, G. Functional Composite Materials Based on Chemically Converted Graphene Adv. Mater. 2011, 23, 1089-1115
    • (2011) Adv. Mater. , vol.23 , pp. 1089-1115
    • Bai, H.1    Li, C.2    Shi, G.3
  • 20
    • 19344375607 scopus 로고    scopus 로고
    • Attachment of organic layers to conductive or semiconductive surfaces by reduction of diazonium salts
    • Pinson, J.; Podvorica, F. Attachment of organic layers to conductive or semiconductive surfaces by reduction of diazonium salts Chem. Soc. Rev. 2005, 34, 429-439
    • (2005) Chem. Soc. Rev. , vol.34 , pp. 429-439
    • Pinson, J.1    Podvorica, F.2
  • 21
    • 77951760229 scopus 로고    scopus 로고
    • Kinetics of Diazonium Functionalization of Chemically Converted Graphene Nanoribbons
    • Sinitskii, A.; Dimiev, A.; Corley, D. A.; Fursina, A. A.; Kosynkin, D. V.; Tour, J. M. Kinetics of Diazonium Functionalization of Chemically Converted Graphene Nanoribbons ACS Nano 2010, 4, 1949-1954
    • (2010) ACS Nano , vol.4 , pp. 1949-1954
    • Sinitskii, A.1    Dimiev, A.2    Corley, D.A.3    Fursina, A.A.4    Kosynkin, D.V.5    Tour, J.M.6
  • 23
    • 76749102992 scopus 로고    scopus 로고
    • Anomalously Large Reactivity of Single Graphene Layers and Edges toward Electron Transfer Chemistries
    • Sharma, R.; Baik, J. H.; Perera, C. J.; Strano, M. S. Anomalously Large Reactivity of Single Graphene Layers and Edges toward Electron Transfer Chemistries Nano Lett. 2010, 10, 398-405
    • (2010) Nano Lett. , vol.10 , pp. 398-405
    • Sharma, R.1    Baik, J.H.2    Perera, C.J.3    Strano, M.S.4
  • 24
    • 80054971109 scopus 로고    scopus 로고
    • Graphene Covalently Binding Aryl Groups: Conductivity Increases Rather than Decreases
    • Huang, P.; Zhu, H.; Jing, L.; Zhao, Y.; Gao, X. Graphene Covalently Binding Aryl Groups: Conductivity Increases Rather than Decreases ACS Nano 2011, 5, 7945-7949
    • (2011) ACS Nano , vol.5 , pp. 7945-7949
    • Huang, P.1    Zhu, H.2    Jing, L.3    Zhao, Y.4    Gao, X.5
  • 27
    • 57149110442 scopus 로고    scopus 로고
    • Diazonium Functionalization of Surfactant-Wrapped Chemically Converted Graphene Sheets
    • Lomeda, J. R.; Doyle, C. D.; Kosynkin, D. V.; Hwang, W.-F.; Tour, J. M. Diazonium Functionalization of Surfactant-Wrapped Chemically Converted Graphene Sheets J. Am. Chem. Soc. 2008, 130, 16201-16206
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 16201-16206
    • Lomeda, J.R.1    Doyle, C.D.2    Kosynkin, D.V.3    Hwang, W.-F.4    Tour, J.M.5
  • 28
    • 77949293427 scopus 로고    scopus 로고
    • Soluble graphene through edge-selective functionalization
    • Sun, Z.; Kohama, S.-i.; Zhang, Z.; Lomeda, J.; Tour, J. Soluble graphene through edge-selective functionalization Nano Res. 2010, 3, 117-125
    • (2010) Nano Res. , vol.3 , pp. 117-125
    • Sun, Z.1    Kohama, S.-I.2    Zhang, Z.3    Lomeda, J.4    Tour, J.5
  • 29
    • 51349157485 scopus 로고    scopus 로고
    • Highly conducting graphene sheets and Langmuir-Blodgett films
    • Li, X.; Zhang, G.; Bai, X.; Sun, X.; Wang, X.; Wang, E.; Dai, H. Highly conducting graphene sheets and Langmuir-Blodgett films Nat. Nano 2008, 3, 538-542
    • (2008) Nat. Nano , vol.3 , pp. 538-542
    • Li, X.1    Zhang, G.2    Bai, X.3    Sun, X.4    Wang, X.5    Wang, E.6    Dai, H.7
  • 32
    • 79959280141 scopus 로고    scopus 로고
    • Sonochemical Preparation of Functionalized Graphenes
    • Xu, H.; Suslick, K. S. Sonochemical Preparation of Functionalized Graphenes J. Am. Chem. Soc. 2011, 133, 9148-9151
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 9148-9151
    • Xu, H.1    Suslick, K.S.2
  • 34
    • 0001136058 scopus 로고
    • Comparison of Phenylcarbene and Phenylnitrene
    • Platz, M. S. Comparison of Phenylcarbene and Phenylnitrene Acc. Chem. Res. 1995, 28, 487-492
    • (1995) Acc. Chem. Res. , vol.28 , pp. 487-492
    • Platz, M.S.1
  • 36
    • 79959444802 scopus 로고    scopus 로고
    • Nitrenes, Carbenes, Diradicals, and Ylides. Interconversions of Reactive Intermediates
    • Wentrup, C. Nitrenes, Carbenes, Diradicals, and Ylides. Interconversions of Reactive Intermediates Acc. Chem. Res. 2011, 44, 393-404
    • (2011) Acc. Chem. Res. , vol.44 , pp. 393-404
    • Wentrup, C.1
  • 37
    • 33749845590 scopus 로고    scopus 로고
    • Kinetics, Spectroscopy, and Computational Chemistry of Arylnitrenes
    • Gritsan, N. P.; Platz, M. S. Kinetics, Spectroscopy, and Computational Chemistry of Arylnitrenes Chem. Rev. 2006, 106, 3844-3867
    • (2006) Chem. Rev. , vol.106 , pp. 3844-3867
    • Gritsan, N.P.1    Platz, M.S.2
  • 41
    • 0000896133 scopus 로고
    • Addition of azides to fullerene C60: Synthesis of azafulleroids
    • Prato, M.; Li, Q. C.; Wudl, F.; Lucchini, V. Addition of azides to fullerene C60: synthesis of azafulleroids J. Am. Chem. Soc. 1993, 115, 1148-1150
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 1148-1150
    • Prato, M.1    Li, Q.C.2    Wudl, F.3    Lucchini, V.4
  • 42
    • 61849159225 scopus 로고    scopus 로고
    • Scalable Functional Group Engineering of Carbon Nanotubes by Improved One-Step Nitrene Chemistry
    • Gao, C.; He, H.; Zhou, L.; Zheng, X.; Zhang, Y. Scalable Functional Group Engineering of Carbon Nanotubes by Improved One-Step Nitrene Chemistry Chem. Mater. 2008, 21, 360-370
    • (2008) Chem. Mater. , vol.21 , pp. 360-370
    • Gao, C.1    He, H.2    Zhou, L.3    Zheng, X.4    Zhang, Y.5
  • 43
    • 33748545580 scopus 로고    scopus 로고
    • Cycloaddition Functionalizations to Preserve or Control the Conductance of Carbon Nanotubes
    • Lee, Y.-S.; Marzari, N. Cycloaddition Functionalizations to Preserve or Control the Conductance of Carbon Nanotubes Phys. Rev. Lett. 2006, 97, 116801/1-116801/4
    • (2006) Phys. Rev. Lett. , vol.97
    • Lee, Y.-S.1    Marzari, N.2
  • 44
    • 67149141615 scopus 로고    scopus 로고
    • Covalent Functionalization of Epitaxial Graphene by Azidotrimethylsilane
    • Choi, J.; Kim, K.-j.; Kim, B.; Lee, H.; Kim, S. Covalent Functionalization of Epitaxial Graphene by Azidotrimethylsilane J. Phys. Chem. C 2009, 113, 9433-9435
    • (2009) J. Phys. Chem. C , vol.113 , pp. 9433-9435
    • Choi, J.1    Kim, K.-J.2    Kim, B.3    Lee, H.4    Kim, S.5
  • 45
    • 77953196994 scopus 로고    scopus 로고
    • Nitrene addition to exfoliated graphene: A one-step route to highly functionalized graphene
    • Strom, T. A.; Dillon, E. P.; Hamilton, C. E.; Barron, A. R. Nitrene addition to exfoliated graphene: a one-step route to highly functionalized graphene Chem. Commun. 2010, 46, 4097-4099
    • (2010) Chem. Commun. , vol.46 , pp. 4097-4099
    • Strom, T.A.1    Dillon, E.P.2    Hamilton, C.E.3    Barron, A.R.4
  • 46
    • 0001391716 scopus 로고
    • Mechanism of intermolecular aromatic substitution by arylnitrenes
    • Abramovitch, R. A.; Challand, S. R.; Scriven, E. F. V. Mechanism of intermolecular aromatic substitution by arylnitrenes J. Am. Chem. Soc. 1972, 94, 1374-1376
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 1374-1376
    • Abramovitch, R.A.1    Challand, S.R.2    Scriven, E.F.V.3
  • 47
    • 37049123077 scopus 로고
    • Studies in azide chemistry. Part V. Synthesis of 4-azido-2,3,5,6- tetrafluoro-, 4-azido-3-chloro-2,5,6-trifluoro-, and 4-azido-3,5-dichloro-2,6- difluoro-pyridine, and some thermal reactions of the tetrafluoro-compound
    • Banks, R. E.; Sparkes, G. R. Studies in azide chemistry. Part V. Synthesis of 4-azido-2,3,5,6-tetrafluoro-, 4-azido-3-chloro-2,5,6-trifluoro-, and 4-azido-3,5-dichloro-2,6-difluoro-pyridine, and some thermal reactions of the tetrafluoro-compound J. Chem. Soc., Perkin Trans. 1 1972, 2964-2970
    • (1972) J. Chem. Soc., Perkin Trans. 1 , pp. 2964-2970
    • Banks, R.E.1    Sparkes, G.R.2
  • 48
    • 0006647917 scopus 로고
    • New reactions of azidopentafluorobenzene; Intermolecular "insertions" into N-H bonds
    • Banks, R. E.; Prakash, A. New reactions of azidopentafluorobenzene; intermolecular "insertions" into N-H bonds Tetrahedron Lett. 1973, 14, 99-102
    • (1973) Tetrahedron Lett. , vol.14 , pp. 99-102
    • Banks, R.E.1    Prakash, A.2
  • 49
    • 37049134648 scopus 로고
    • Studies in azide chemistry. Part VI. Some reactions of perfluoroazidobenzene and perfluoro-4-azidotoluene
    • Banks, R. E.; Prakash, A. Studies in azide chemistry. Part VI. Some reactions of perfluoroazidobenzene and perfluoro-4-azidotoluene J. Chem. Soc., Perkin Trans. 1 1974, 1365-1371
    • (1974) J. Chem. Soc., Perkin Trans. 1 , pp. 1365-1371
    • Banks, R.E.1    Prakash, A.2
  • 51
    • 37049111789 scopus 로고
    • Decisive evidence for the occurrence of ring-expansion during pyrolysis of azidopentafluorobenzene: X-ray crystallographic analysis of 'pentafluorophenylnitrene dimer'
    • Banks, R. E.; Venayak, N. D.; Hamor, T. A. Decisive evidence for the occurrence of ring-expansion during pyrolysis of azidopentafluorobenzene: X-ray crystallographic analysis of 'pentafluorophenylnitrene dimer' J. Chem. Soc., Chem. Commun. 1980, 900-901
    • (1980) J. Chem. Soc., Chem. Commun. , pp. 900-901
    • Banks, R.E.1    Venayak, N.D.2    Hamor, T.A.3
  • 52
    • 46549091322 scopus 로고
    • Studies in azide chemistry. Part 13 [1]. Intermolecular insertion of azide-derived polyfluorinated aryl- and heteroaryl-nitrenes into ring C·H bonds of 1,3, 5-trimethyl- and 1,3,5-trimethoxy-benzene
    • Banks, R. E.; Madany, I. M. Studies in azide chemistry. Part 13 [1]. Intermolecular insertion of azide-derived polyfluorinated aryl- and heteroaryl-nitrenes into ring C·H bonds of 1,3, 5-trimethyl- and 1,3,5-trimethoxy-benzene J. Fluorine Chem. 1985, 30, 211-226
    • (1985) J. Fluorine Chem. , vol.30 , pp. 211-226
    • Banks, R.E.1    Madany, I.M.2
  • 53
    • 0027203297 scopus 로고
    • New Photolabeling and Crosslinking Methods
    • Brunner, J. New Photolabeling and Crosslinking Methods Annu. Rev. Biochem. 1993, 62, 483-514
    • (1993) Annu. Rev. Biochem. , vol.62 , pp. 483-514
    • Brunner, J.1
  • 55
    • 0027572579 scopus 로고
    • Exploratory photochemistry of fluorinated aryl azides. Implications for the design of photoaffinity labeling reagents
    • Schnapp, K. A.; Poe, R.; Leyva, E.; Soundararajan, N.; Platz, M. S. Exploratory photochemistry of fluorinated aryl azides. Implications for the design of photoaffinity labeling reagents Bioconjugate Chem. 1993, 4, 172-177
    • (1993) Bioconjugate Chem. , vol.4 , pp. 172-177
    • Schnapp, K.A.1    Poe, R.2    Leyva, E.3    Soundararajan, N.4    Platz, M.S.5
  • 56
    • 45149142005 scopus 로고
    • Functionalized Perfluorophenyl Azides: New Reagents for Photoaffinity Labeling
    • Keana, J. F. W.; Xiong Cai, S. Functionalized Perfluorophenyl Azides: New Reagents for Photoaffinity Labeling J. Fluorine Chem. 1989, 43, 151-154
    • (1989) J. Fluorine Chem. , vol.43 , pp. 151-154
    • Keana, J.F.W.1    Xiong Cai, S.2
  • 57
    • 0000584363 scopus 로고
    • New reagents for photoaffinity labeling: Synthesis and photolysis of functionalized perfluorophenyl azides
    • Keana, J. F. W.; Cai, S. X. New reagents for photoaffinity labeling: synthesis and photolysis of functionalized perfluorophenyl azides J. Org. Chem. 1990, 55, 3640-3647
    • (1990) J. Org. Chem. , vol.55 , pp. 3640-3647
    • Keana, J.F.W.1    Cai, S.X.2
  • 58
    • 0000281599 scopus 로고
    • Toward the development of radiolabeled fluorophenyl azide-based photolabeling reagents: Synthesis and photolysis of iodinated 4-azidoperfluorobenzoates and 4-azido-3,5,6-trifluorobenzoates
    • Cai, S. X.; Glenn, D. J.; Keana, J. F. W. Toward the development of radiolabeled fluorophenyl azide-based photolabeling reagents: synthesis and photolysis of iodinated 4-azidoperfluorobenzoates and 4-azido-3,5,6- trifluorobenzoates J. Org. Chem. 1992, 57, 1299-1304
    • (1992) J. Org. Chem. , vol.57 , pp. 1299-1304
    • Cai, S.X.1    Glenn, D.J.2    Keana, J.F.W.3
  • 59
    • 0035797856 scopus 로고    scopus 로고
    • Fabrication of polymer thin films and arrays with spatial and topographical controls
    • Bartlett, M. A.; Yan, M. Fabrication of polymer thin films and arrays with spatial and topographical controls Adv. Mater. (Weinheim, Ger.) 2001, 13, 1449-1451
    • (2001) Adv. Mater. (Weinheim, Ger.) , vol.13 , pp. 1449-1451
    • Bartlett, M.A.1    Yan, M.2
  • 60
    • 0012343396 scopus 로고    scopus 로고
    • Micro/nanowell arrays fabricated from covalently immobilized polymer thin films on a flat substrate
    • Yan, M.; Bartlett, M. A. Micro/nanowell arrays fabricated from covalently immobilized polymer thin films on a flat substrate Nano Lett. 2002, 2, 275-278
    • (2002) Nano Lett. , vol.2 , pp. 275-278
    • Yan, M.1    Bartlett, M.A.2
  • 61
    • 12744262869 scopus 로고    scopus 로고
    • Covalent immobilization of polypropylene thin films
    • Yan, M.; Ren, J. Covalent immobilization of polypropylene thin films J. Mater. Chem. 2005, 15, 523-527
    • (2005) J. Mater. Chem. , vol.15 , pp. 523-527
    • Yan, M.1    Ren, J.2
  • 62
    • 33749031030 scopus 로고    scopus 로고
    • A General Approach to the Covalent Immobilization of Single Polymers
    • Liu, L.; Yan, M. A General Approach to the Covalent Immobilization of Single Polymers Angew. Chem., Int. Ed. 2006, 45, 6207-6210
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 6207-6210
    • Liu, L.1    Yan, M.2
  • 63
    • 34250337665 scopus 로고    scopus 로고
    • Photochemically initiated single polymer immobilization
    • Yan, M. Photochemically initiated single polymer immobilization Chem.-Eur. J. 2007, 13, 4138-4144
    • (2007) Chem. - Eur. J. , vol.13 , pp. 4138-4144
    • Yan, M.1
  • 64
    • 44649085051 scopus 로고    scopus 로고
    • A Versatile Method for Grafting Polymers on Nanoparticles
    • Gann, J. P.; Yan, M. A Versatile Method for Grafting Polymers on Nanoparticles Langmuir 2008, 24, 5319-5323
    • (2008) Langmuir , vol.24 , pp. 5319-5323
    • Gann, J.P.1    Yan, M.2
  • 65
    • 78650174340 scopus 로고    scopus 로고
    • Fabrication and anti-fouling properties of photochemically and thermally immobilized poly(ethylene oxide) and low molecular weight poly(ethylene glycol) thin films
    • Wang, H.; Ren, J.; Hlaing, A.; Yan, M. Fabrication and anti-fouling properties of photochemically and thermally immobilized poly(ethylene oxide) and low molecular weight poly(ethylene glycol) thin films J. Colloid Interface Sci. 2011, 354, 160-167
    • (2011) J. Colloid Interface Sci. , vol.354 , pp. 160-167
    • Wang, H.1    Ren, J.2    Hlaing, A.3    Yan, M.4
  • 66
    • 84862832882 scopus 로고    scopus 로고
    • Evaluation of photochemically immobilized poly(2-ethyl-2-oxazoline) thin films as protein-resistant surfaces
    • Wang, H.; Li, L.; Tong, Q.; Yan, M. Evaluation of photochemically immobilized poly(2-ethyl-2-oxazoline) thin films as protein-resistant surfaces ACS Appl. Mater. Interfaces 2011, 3, 3463-3471
    • (2011) ACS Appl. Mater. Interfaces , vol.3 , pp. 3463-3471
    • Wang, H.1    Li, L.2    Tong, Q.3    Yan, M.4
  • 67
    • 67650687353 scopus 로고    scopus 로고
    • Photoinitiated Coupling of Unmodified Monosaccharides to Iron Oxide Nanoparticles for Sensing Proteins and Bacteria
    • Liu, L.-H.; Dietsch, H.; Schurtenberger, P.; Yan, M. Photoinitiated Coupling of Unmodified Monosaccharides to Iron Oxide Nanoparticles for Sensing Proteins and Bacteria Bioconjugate Chem. 2009, 20, 1349-1355
    • (2009) Bioconjugate Chem. , vol.20 , pp. 1349-1355
    • Liu, L.-H.1    Dietsch, H.2    Schurtenberger, P.3    Yan, M.4
  • 68
    • 77951961399 scopus 로고    scopus 로고
    • Glyconanomaterials: Synthesis, Characterization, and Ligand Presentation
    • Wang, X.; Ramstroem, O.; Yan, M. Glyconanomaterials: Synthesis, Characterization, and Ligand Presentation Adv. Mater. (Weinheim, Ger.) 2010, 22, 1946-1953
    • (2010) Adv. Mater. (Weinheim, Ger.) , vol.22 , pp. 1946-1953
    • Wang, X.1    Ramstroem, O.2    Yan, M.3
  • 69
    • 78049496531 scopus 로고    scopus 로고
    • Quantitative Analysis of Multivalent Ligand Presentation on Gold Glyconanoparticles and the Impact on Lectin Binding
    • Wang, X.; Ramstrom, O.; Yan, M. Quantitative Analysis of Multivalent Ligand Presentation on Gold Glyconanoparticles and the Impact on Lectin Binding Anal. Chem. (Washington, DC, U. S.) 2010, 82, 9082-9089
    • (2010) Anal. Chem. (Washington, DC, U. S.) , vol.82 , pp. 9082-9089
    • Wang, X.1    Ramstrom, O.2    Yan, M.3
  • 70
    • 67650097592 scopus 로고    scopus 로고
    • Covalent Immobilization of Antibacterial Furanones via Photochemical Activation of Perfluorophenylazide
    • Al-Bataineh, S. A.; Luginbuehl, R.; Textor, M.; Yan, M. Covalent Immobilization of Antibacterial Furanones via Photochemical Activation of Perfluorophenylazide Langmuir 2009, 25, 7432-7437
    • (2009) Langmuir , vol.25 , pp. 7432-7437
    • Al-Bataineh, S.A.1    Luginbuehl, R.2    Textor, M.3    Yan, M.4
  • 71
    • 79960798835 scopus 로고    scopus 로고
    • Polymer-based photocoupling agent for the efficient immobilization of nanomaterials and small molecules
    • Kubo, T.; Wang, X.; Tong, Q.; Yan, M. Polymer-based photocoupling agent for the efficient immobilization of nanomaterials and small molecules Langmuir 2011, 27, 9372-9378
    • (2011) Langmuir , vol.27 , pp. 9372-9378
    • Kubo, T.1    Wang, X.2    Tong, Q.3    Yan, M.4
  • 72
    • 5744250048 scopus 로고
    • Photochemical and Thermal Reactions of C60 with N-Succinimidyl 4-Azido-2,3,5,6-tetrafluorobenzoate: A New Method for Functionalization of C60
    • Yan, M.; Cai, S. X.; Keana, J. F. W. Photochemical and Thermal Reactions of C60 with N-Succinimidyl 4-Azido-2,3,5,6-tetrafluorobenzoate: A New Method for Functionalization of C60 J. Org. Chem. 1994, 59, 5951-5954
    • (1994) J. Org. Chem. , vol.59 , pp. 5951-5954
    • Yan, M.1    Cai, S.X.2    Keana, J.F.W.3
  • 73
    • 70349967898 scopus 로고    scopus 로고
    • Simple Method for the Covalent Immobilization of Graphene
    • Liu, L.-H.; Yan, M. Simple Method for the Covalent Immobilization of Graphene Nano Lett. 2009, 9, 3375-3378
    • (2009) Nano Lett. , vol.9 , pp. 3375-3378
    • Liu, L.-H.1    Yan, M.2
  • 74
    • 77956425479 scopus 로고    scopus 로고
    • Derivatization of Pristine Graphene with Well-Defined Chemical Functionalities
    • Liu, L.-H.; Lerner, M. M.; Yan, M. Derivatization of Pristine Graphene with Well-Defined Chemical Functionalities Nano Lett. 2010, 10, 3754-3756
    • (2010) Nano Lett. , vol.10 , pp. 3754-3756
    • Liu, L.-H.1    Lerner, M.M.2    Yan, M.3
  • 75
    • 79951864030 scopus 로고    scopus 로고
    • Functionalization of pristine graphene with perfluorophenyl azides
    • Liu, L.-H.; Yan, M. Functionalization of pristine graphene with perfluorophenyl azides J. Mater. Chem. 2011, 21, 3273-3276
    • (2011) J. Mater. Chem. , vol.21 , pp. 3273-3276
    • Liu, L.-H.1    Yan, M.2
  • 76
    • 78649300661 scopus 로고    scopus 로고
    • Perfluorophenyl Azides: New Applications in Surface Functionalization and Nanomaterial Synthesis
    • Liu, L.-H.; Yan, M. Perfluorophenyl Azides: New Applications in Surface Functionalization and Nanomaterial Synthesis Acc. Chem. Res. 2010, 43, 1434-1443
    • (2010) Acc. Chem. Res. , vol.43 , pp. 1434-1443
    • Liu, L.-H.1    Yan, M.2
  • 78
    • 84860799232 scopus 로고    scopus 로고
    • Introducing dichlorocarbene in graphene
    • Chua, C. K.; Ambrosi, A.; Pumera, M. Introducing dichlorocarbene in graphene Chem. Commun. 2012, 48, 5376-5378
    • (2012) Chem. Commun. , vol.48 , pp. 5376-5378
    • Chua, C.K.1    Ambrosi, A.2    Pumera, M.3
  • 79
    • 80054885349 scopus 로고    scopus 로고
    • Light-Activated Covalent Formation of Gold Nanoparticle-Graphene and Gold Nanoparticle-Glass Composites
    • Ismaili, H.; Geng, D.; Sun, A. X.; Kantzas, T. T.; Workentin, M. S. Light-Activated Covalent Formation of Gold Nanoparticle-Graphene and Gold Nanoparticle-Glass Composites Langmuir 2011, 27, 13261-13268
    • (2011) Langmuir , vol.27 , pp. 13261-13268
    • Ismaili, H.1    Geng, D.2    Sun, A.X.3    Kantzas, T.T.4    Workentin, M.S.5
  • 80
    • 33947449575 scopus 로고
    • Carbon Dichloride as an Intermediate in the Basic Hydrolysis of Chloroform. A Mechanism for Substitution Reactions at a Saturated Carbon Atom
    • Hine, J. Carbon Dichloride as an Intermediate in the Basic Hydrolysis of Chloroform. A Mechanism for Substitution Reactions at a Saturated Carbon Atom J. Am. Chem. Soc. 1950, 72, 2438-2445
    • (1950) J. Am. Chem. Soc. , vol.72 , pp. 2438-2445
    • Hine, J.1
  • 81
    • 0019332445 scopus 로고
    • 3-Trifluoromethyl-3-phenyldiazirine. A new carbene generating group for photolabeling reagents
    • Brunner, J.; Senn, H.; Richards, F. M. 3-Trifluoromethyl-3- phenyldiazirine. A new carbene generating group for photolabeling reagents J. Biol. Chem. 1980, 255, 3313-3318
    • (1980) J. Biol. Chem. , vol.255 , pp. 3313-3318
    • Brunner, J.1    Senn, H.2    Richards, F.M.3
  • 82
    • 0034309923 scopus 로고    scopus 로고
    • Photoactivatable Reagents Based on Aryl(trifluoromethyl)diazirines: Synthesis and Application for Studying Nucleic Acid-Protein Interactions
    • Korshunova, G. A.; Sumbatyan, N. V.; Topin, A. N.; Mtchedlidze, M. T. Photoactivatable Reagents Based on Aryl(trifluoromethyl)diazirines: Synthesis and Application for Studying Nucleic Acid-Protein Interactions Mol. Biol. 2000, 34, 823-839
    • (2000) Mol. Biol. , vol.34 , pp. 823-839
    • Korshunova, G.A.1    Sumbatyan, N.V.2    Topin, A.N.3    Mtchedlidze, M.T.4
  • 83
    • 80051710777 scopus 로고    scopus 로고
    • 3-Aryl-3-(trifluoromethyl)diazirines as Versatile Photoactivated "linker" Molecules for the Improved Covalent Modification of Graphitic and Carbon Nanotube Surfaces
    • Lawrence, E. J.; Wildgoose, G. G.; Aldous, L.; Wu, Y. A.; Warner, J. H.; Compton, R. G.; McNaughter, P. D. 3-Aryl-3-(trifluoromethyl)diazirines as Versatile Photoactivated "Linker" Molecules for the Improved Covalent Modification of Graphitic and Carbon Nanotube Surfaces Chem. Mater. 2011, 23, 3740-3751
    • (2011) Chem. Mater. , vol.23 , pp. 3740-3751
    • Lawrence, E.J.1    Wildgoose, G.G.2    Aldous, L.3    Wu, Y.A.4    Warner, J.H.5    Compton, R.G.6    McNaughter, P.D.7
  • 84
    • 79952751811 scopus 로고    scopus 로고
    • Covalently Assembled Gold Nanoparticle-Carbon Nanotube Hybrids via a Photoinitiated Carbene Addition Reaction
    • Ismaili, H.; Lagugné-Labarthet, F. o.; Workentin, M. S. Covalently Assembled Gold Nanoparticle-Carbon Nanotube Hybrids via a Photoinitiated Carbene Addition Reaction Chem. Mater. 2011, 23, 1519-1525
    • (2011) Chem. Mater. , vol.23 , pp. 1519-1525
    • Ismaili, H.1    F, O.L.2    Workentin, M.S.3
  • 85
    • 79959786828 scopus 로고    scopus 로고
    • Covalent diamond-gold nanojewel hybrids via photochemically generated carbenes
    • Ismaili, H.; Workentin, M. S. Covalent diamond-gold nanojewel hybrids via photochemically generated carbenes Chem. Commun. 2011, 47, 7788-7790
    • (2011) Chem. Commun. , vol.47 , pp. 7788-7790
    • Ismaili, H.1    Workentin, M.S.2
  • 88
    • 84856852491 scopus 로고    scopus 로고
    • Chemical Understanding of Carbide Cluster Metallofullerenes: A Case Study on Sc2C2@C2v(5)-C80 with Complete X-ray Crystallographic Characterizations
    • Kurihara, H.; Lu, X.; Iiduka, Y.; Nikawa, H.; Mizorogi, N.; Slanina, Z.; Tsuchiya, T.; Nagase, S.; Akasaka, T. Chemical Understanding of Carbide Cluster Metallofullerenes: A Case Study on Sc2C2@C2v(5)-C80 with Complete X-ray Crystallographic Characterizations J. Am. Chem. Soc. 2012, 134, 3139-3144
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 3139-3144
    • Kurihara, H.1    Lu, X.2    Iiduka, Y.3    Nikawa, H.4    Mizorogi, N.5    Slanina, Z.6    Tsuchiya, T.7    Nagase, S.8    Akasaka, T.9
  • 89
    • 77956570125 scopus 로고    scopus 로고
    • Diazirine-Modified Gold Nanoparticle: Template for Efficient Photoinduced Interfacial Carbene Insertion Reactions
    • Ismaili, H.; Lee, S.; Workentin, M. S. Diazirine-Modified Gold Nanoparticle: Template for Efficient Photoinduced Interfacial Carbene Insertion Reactions Langmuir 2010, 26, 14958-14964
    • (2010) Langmuir , vol.26 , pp. 14958-14964
    • Ismaili, H.1    Lee, S.2    Workentin, M.S.3
  • 90
    • 0032542719 scopus 로고    scopus 로고
    • Benzyne Adds Across a Closed 5-6 Ring Fusion in C70: Evidence for Bond Delocalization in Fullerenes
    • Meier, M. S.; Wang, G.-W.; Haddon, R. C.; Brock, C. P.; Lloyd, M. A.; Selegue, J. P. Benzyne Adds Across a Closed 5-6 Ring Fusion in C70: Evidence for Bond Delocalization in Fullerenes J. Am. Chem. Soc. 1998, 120, 2337-2342
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 2337-2342
    • Meier, M.S.1    Wang, G.-W.2    Haddon, R.C.3    Brock, C.P.4    Lloyd, M.A.5    Selegue, J.P.6
  • 91
    • 74549146902 scopus 로고    scopus 로고
    • Nitrated Benzyne Derivatives of La@C82: Addition of NO2 and Its Positional Directing Effect on the Subsequent Addition of Benzynes
    • Lu, X.; Nikawa, H.; Tsuchiya, T.; Akasaka, T.; Toki, M.; Sawa, H.; Mizorogi, N.; Nagase, S. Nitrated Benzyne Derivatives of La@C82: Addition of NO2 and Its Positional Directing Effect on the Subsequent Addition of Benzynes Angew. Chem., Int. Ed. 2010, 49, 594-597
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 594-597
    • Lu, X.1    Nikawa, H.2    Tsuchiya, T.3    Akasaka, T.4    Toki, M.5    Sawa, H.6    Mizorogi, N.7    Nagase, S.8
  • 92
    • 1642414364 scopus 로고    scopus 로고
    • Addition of Benzyne to Gd@C82
    • Lu, X.; Xu, J.; He, X.; Shi, Z.; Gu, Z. Addition of Benzyne to Gd@C82 Chem. Mater. 2004, 16, 953-955
    • (2004) Chem. Mater. , vol.16 , pp. 953-955
    • Lu, X.1    Xu, J.2    He, X.3    Shi, Z.4    Gu, Z.5
  • 93
    • 79551702834 scopus 로고    scopus 로고
    • [2 + 2] Cycloaddition Reaction to Sc3N@Ih-C80. The Formation of Very Stable [5,6]- and [6,6]-Adducts
    • Li, F.-F.; Pinzón, J. R.; Mercado, B. Q.; Olmstead, M. M.; Balch, A. L.; Echegoyen, L. [2 + 2] Cycloaddition Reaction to Sc3N@Ih-C80. The Formation of Very Stable [5,6]- and [6,6]-Adducts J. Am. Chem. Soc. 2011, 133, 1563-1571
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 1563-1571
    • Li, F.-F.1    Pinzón, J.R.2    Mercado, B.Q.3    Olmstead, M.M.4    Balch, A.L.5    Echegoyen, L.6
  • 94
    • 77957670391 scopus 로고    scopus 로고
    • Aryne cycloaddition: Highly efficient chemical modification of graphene
    • Zhong, X.; Jin, J.; Li, S.; Niu, Z.; Hu, W.; Li, R.; Ma, J. Aryne cycloaddition: highly efficient chemical modification of graphene Chem. Commun. 2010, 46, 7340-7342
    • (2010) Chem. Commun. , vol.46 , pp. 7340-7342
    • Zhong, X.1    Jin, J.2    Li, S.3    Niu, Z.4    Hu, W.5    Li, R.6    Ma, J.7


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