메뉴 건너뛰기




Volumn 30, Issue 1, 2014, Pages 172-178

Multifunctional silicon surfaces: Reaction of dichlorocarbene generated from seyferth reagent with hydrogen-terminated silicon (111) surfaces

Author keywords

[No Author keywords available]

Indexed keywords

DICHLOROCARBENE; GRIGNARD REAGENT; HYDROGEN-TERMINATED SILICON; MOLECULAR TRANSFORMATION; SILICON (111) SURFACE; SILICON CARBON; SILICON SURFACES; SURFACE BOUNDS;

EID: 84892611152     PISSN: 07437463     EISSN: 15205827     Source Type: Journal    
DOI: 10.1021/la403789a     Document Type: Article
Times cited : (7)

References (58)
  • 2
    • 84863474819 scopus 로고    scopus 로고
    • Hybrids of organic molecules and flat, oxide-free silicon: High-density monolayers, electronic properties, and functionalization
    • Li, Y.; Calder, S.; Yaffe, O.; Cahen, D.; Haick, H.; Kronik, L.; Zuilhof, H. Hybrids of organic molecules and flat, oxide-free silicon: high-density monolayers, electronic properties, and functionalization Langmuir 2012, 28, 9920-9929
    • (2012) Langmuir , vol.28 , pp. 9920-9929
    • Li, Y.1    Calder, S.2    Yaffe, O.3    Cahen, D.4    Haick, H.5    Kronik, L.6    Zuilhof, H.7
  • 6
    • 0034673351 scopus 로고    scopus 로고
    • Synthesis and characterization of DNA-modified silicon (111) surfaces
    • Strother, T.; Cai, W.; Zhao, X.; Hamers, R. J.; Smith, L. M. Synthesis and characterization of DNA-modified silicon (111) surfaces J. Am. Chem. Soc. 2000, 122, 1205-1209
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 1205-1209
    • Strother, T.1    Cai, W.2    Zhao, X.3    Hamers, R.J.4    Smith, L.M.5
  • 9
    • 78049333550 scopus 로고    scopus 로고
    • High-performance photoelectrochemical cells from ionic liquid electrolyte in methyl-terminated silicon nanowire arrays
    • Shen, X.; Sun, B.; Yan, F.; Zhao, J.; Zhang, F.; Wang, S.; Zhu, X.; Lee, S. High-performance photoelectrochemical cells from ionic liquid electrolyte in methyl-terminated silicon nanowire arrays ACS Nano 2010, 4, 5869-5876
    • (2010) ACS Nano , vol.4 , pp. 5869-5876
    • Shen, X.1    Sun, B.2    Yan, F.3    Zhao, J.4    Zhang, F.5    Wang, S.6    Zhu, X.7    Lee, S.8
  • 10
    • 59349092385 scopus 로고    scopus 로고
    • Toward metal-organic insulator-semiconductor solar cells, based on molecular monolayer self-assembly on n-Si
    • Har-Lavan, R.; Ron, I.; Thieblemont, F.; Cahen, D. Toward metal-organic insulator-semiconductor solar cells, based on molecular monolayer self-assembly on n-Si Appl. Phys. Lett. 2009, 94, 043308-043311
    • (2009) Appl. Phys. Lett. , vol.94 , pp. 043308-043311
    • Har-Lavan, R.1    Ron, I.2    Thieblemont, F.3    Cahen, D.4
  • 11
    • 77952861198 scopus 로고    scopus 로고
    • Wet chemical routes to the assembly of organic monolayers on silicon surfaces via the formation of Si-C bonds: Surface preparation, passivation and functionalization
    • Ciampi, S.; Harper, J. B.; Gooding, J. J. Wet chemical routes to the assembly of organic monolayers on silicon surfaces via the formation of Si-C bonds: surface preparation, passivation and functionalization Chem. Soc. Rev. 2010, 39, 2158-2183
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 2158-2183
    • Ciampi, S.1    Harper, J.B.2    Gooding, J.J.3
  • 12
    • 0036589258 scopus 로고    scopus 로고
    • Organometallic chemistry on silicon and germanium surfaces
    • Buriak, J. M. Organometallic chemistry on silicon and germanium surfaces Chem. Rev. 2002, 102, 1271-1308
    • (2002) Chem. Rev. , vol.102 , pp. 1271-1308
    • Buriak, J.M.1
  • 13
    • 84872110861 scopus 로고    scopus 로고
    • Silicon surface functionalization targeting Si-N linkages
    • Tian, F.; Teplyakov, A. V. Silicon surface functionalization targeting Si-N linkages Langmuir 2012, 29, 13-28
    • (2012) Langmuir , vol.29 , pp. 13-28
    • Tian, F.1    Teplyakov, A.V.2
  • 14
    • 0029274673 scopus 로고
    • Alkyl monolayers on silicon prepared from 1-alkenes and hydrogen-terminated silicon
    • Linford, M. R.; Fenter, P.; Eisenberger, P. M.; Chidsey, C. E. D. Alkyl monolayers on silicon prepared from 1-alkenes and hydrogen-terminated silicon J. Am. Chem. Soc. 1995, 117, 3145-3155
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 3145-3155
    • Linford, M.R.1    Fenter, P.2    Eisenberger, P.M.3    Chidsey, C.E.D.4
  • 16
    • 0345055314 scopus 로고    scopus 로고
    • Photoactivated preparation and patterning of self-assembled monolayers with 1-alkenes and aldehydes on silicon hydride surfaces
    • Effenberger, F.; Götz, G.; Bidlingmaier, B.; Wezstein, M. Photoactivated preparation and patterning of self-assembled monolayers with 1-alkenes and aldehydes on silicon hydride surfaces Angew. Chem., Int. Ed. 1998, 37, 2462-2464
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 2462-2464
    • Effenberger, F.1    Götz, G.2    Bidlingmaier, B.3    Wezstein, M.4
  • 17
    • 0032542258 scopus 로고    scopus 로고
    • Photopatterned hydrosilylation on porous silicon
    • Stewart, M. P.; Buriak, J. M. Photopatterned hydrosilylation on porous silicon Angew. Chem., Int. Ed. 1998, 37, 3257-3260
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 3257-3260
    • Stewart, M.P.1    Buriak, J.M.2
  • 18
    • 0034205444 scopus 로고    scopus 로고
    • Photoreactivity of unsaturated compounds with hydrogen-terminated silicon(111)
    • Cicero, R. L.; Linford, M. R.; Chidsey, C. E. D. Photoreactivity of unsaturated compounds with hydrogen-terminated silicon(111) Langmuir 2000, 16, 5688-5695
    • (2000) Langmuir , vol.16 , pp. 5688-5695
    • Cicero, R.L.1    Linford, M.R.2    Chidsey, C.E.D.3
  • 19
    • 0034802459 scopus 로고    scopus 로고
    • Exciton-mediated hydrosilylation on photoluminescent nanocrystalline silicon
    • Stewart, M. P.; Buriak, J. M. Exciton-mediated hydrosilylation on photoluminescent nanocrystalline silicon J. Am. Chem. Soc. 2001, 123, 7821-7830
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 7821-7830
    • Stewart, M.P.1    Buriak, J.M.2
  • 21
    • 74049097537 scopus 로고    scopus 로고
    • Comparing the reactivity of alkynes and alkenes on silicon (100) surfaces
    • Ng, A.; Ciampi, S.; James, M.; Harper, J. B.; Gooding, J. J. Comparing the reactivity of alkynes and alkenes on silicon (100) surfaces Langmuir 2009, 25, 13934-13941
    • (2009) Langmuir , vol.25 , pp. 13934-13941
    • Ng, A.1    Ciampi, S.2    James, M.3    Harper, J.B.4    Gooding, J.J.5
  • 22
    • 0000807285 scopus 로고    scopus 로고
    • Lewis acid mediated functionalization of porous silicon with substituted alkenes and alkynes
    • Buriak, J. M.; Allen, M. J. Lewis acid mediated functionalization of porous silicon with substituted alkenes and alkynes J. Am. Chem. Soc. 1998, 120, 1339-1340
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1339-1340
    • Buriak, J.M.1    Allen, M.J.2
  • 24
    • 79957679992 scopus 로고    scopus 로고
    • Mild and efficient functionalization of hydrogen-terminated Si(111) via sonochemical activated hydrosilylation
    • Zhong, Y. L.; Bernasek, S. L. Mild and efficient functionalization of hydrogen-terminated Si(111) via sonochemical activated hydrosilylation J. Am. Chem. Soc. 2011, 133, 8118-8121
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 8118-8121
    • Zhong, Y.L.1    Bernasek, S.L.2
  • 26
    • 0035815017 scopus 로고    scopus 로고
    • Formation of covalently attached polymer overlayers on Si(111) surfaces using ring-opening metathesis polymerization methods
    • Juang, A.; Scherman, O. A.; Grubbs, R. H.; Lewis, N. S. Formation of covalently attached polymer overlayers on Si(111) surfaces using ring-opening metathesis polymerization methods Langmuir 2001, 17, 1321-1323
    • (2001) Langmuir , vol.17 , pp. 1321-1323
    • Juang, A.1    Scherman, O.A.2    Grubbs, R.H.3    Lewis, N.S.4
  • 27
    • 33746933808 scopus 로고    scopus 로고
    • Covalent attachment of acetylene and methylacetylene functionality to Si(111) surfaces: Scaffolds for organic surface functionalization while retaining Si-C passivation of Si(111) surface sites
    • Hurley, P. T.; Nemanick, E. J.; Brunschwig, B. S.; Lewis, N. S. Covalent attachment of acetylene and methylacetylene functionality to Si(111) surfaces: scaffolds for organic surface functionalization while retaining Si-C passivation of Si(111) surface sites J. Am. Chem. Soc. 2006, 128, 9990-9991
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9990-9991
    • Hurley, P.T.1    Nemanick, E.J.2    Brunschwig, B.S.3    Lewis, N.S.4
  • 28
    • 41749111146 scopus 로고    scopus 로고
    • Passivation and secondary functionalization of allyl-terminated Si(111) surfaces
    • Plass, K. E.; Liu, X.; Brunschwig, B. S.; Lewis, N. S. Passivation and secondary functionalization of allyl-terminated Si(111) surfaces Chem. Mater. 2008, 20, 2228-2233
    • (2008) Chem. Mater. , vol.20 , pp. 2228-2233
    • Plass, K.E.1    Liu, X.2    Brunschwig, B.S.3    Lewis, N.S.4
  • 30
    • 47749133849 scopus 로고    scopus 로고
    • Highly stable organic modification of Si(111) surfaces: Towards reacting Si with further functionalities while preserving the desirable chemical properties of full Si-C atop site terminations
    • Puniredd, S. R.; Assad, O.; Haick, H. Highly stable organic modification of Si(111) surfaces: towards reacting Si with further functionalities while preserving the desirable chemical properties of full Si-C atop site terminations J. Am. Chem. Soc. 2008, 130, 9184-9185
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 9184-9185
    • Puniredd, S.R.1    Assad, O.2    Haick, H.3
  • 31
    • 67749135593 scopus 로고    scopus 로고
    • Stable scaffolds for reacting Si nanowires with further organic functionalities while preserving Si-C passivation of surface sites
    • Assad, O.; Puniredd, S. R.; Stelzner, T.; Christiansen, S.; Haick, H. Stable scaffolds for reacting Si nanowires with further organic functionalities while preserving Si-C passivation of surface sites J. Am. Chem. Soc. 2008, 130, 17670-17671
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 17670-17671
    • Assad, O.1    Puniredd, S.R.2    Stelzner, T.3    Christiansen, S.4    Haick, H.5
  • 32
    • 53849125061 scopus 로고    scopus 로고
    • Highly stable organic monolayers for reacting silicon with further functionalities: The effect of the C-C Bond nearest the silicon surface
    • Puniredd, S. R.; Assad, O.; Haick, H. Highly stable organic monolayers for reacting silicon with further functionalities: the effect of the C-C Bond nearest the silicon surface J. Am. Chem. Soc. 2008, 130, 13727-13734
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 13727-13734
    • Puniredd, S.R.1    Assad, O.2    Haick, H.3
  • 33
    • 2142772866 scopus 로고
    • The preparation of dihalomethyl derivatives of carbon, silicon, and germanium by the action of phenyl-(trihalomethyl)mercurials on C-H, Si-H, and Ge-H linkages
    • Seyferth, D.; Burlitch, J. M. The preparation of dihalomethyl derivatives of carbon, silicon, and germanium by the action of phenyl-(trihalomethyl) mercurials on C-H, Si-H, and Ge-H linkages J. Am. Chem. Soc. 1963, 85, 2667-2668
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 2667-2668
    • Seyferth, D.1    Burlitch, J.M.2
  • 34
    • 0001091348 scopus 로고
    • Halomethyl-metal compounds X. The reaction of organosilicon, organogermanium and organotin hydrides with phenyl(trihalomethyl)mercury compounds
    • Seyferth, D.; Burlitch, J. M.; Dertouzos, H.; Simmons, H. D., Jr. Halomethyl-metal compounds X. The reaction of organosilicon, organogermanium and organotin hydrides with phenyl(trihalomethyl)mercury compounds J. Organomet. Chem. 1967, 7, 405-413
    • (1967) J. Organomet. Chem. , vol.7 , pp. 405-413
    • Seyferth, D.1    Burlitch, J.M.2    Dertouzos, H.3    Simmons, Jr.H.D.4
  • 35
    • 0042207132 scopus 로고
    • Halomethylmetal compounds. XVII. The mechanism of dichlorocarbene insertion into the Si-H bond by the mercurial route
    • Seyferth, D.; Damrauer, R.; Mui, J. Y.-P.; Jula, T. F. Halomethylmetal compounds. XVII. The mechanism of dichlorocarbene insertion into the Si-H bond by the mercurial route J. Am. Chem. Soc. 1968, 90, 2944-2948
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 2944-2948
    • Seyferth, D.1    Damrauer, R.2    Mui, J.Y.-P.3    Jula, T.F.4
  • 36
    • 0002850767 scopus 로고
    • Halomethyl-metal compounds XX. An improved synthesis of phenyl(trihalomethyl)mercury compounds
    • Seyferth, D.; Lambert, R. L., Jr. Halomethyl-metal compounds XX. An improved synthesis of phenyl(trihalomethyl)mercury compounds J. Organomet. Chem. 1969, 16, 21-26
    • (1969) J. Organomet. Chem. , vol.16 , pp. 21-26
    • Seyferth, D.1    Lambert, Jr.R.L.2
  • 37
    • 84871397353 scopus 로고    scopus 로고
    • A new method to generate arene-terminated Si(111) and Ge(111) surfaces via a palladium-catalyzed arylation reaction
    • Yamanoi, Y.; Sendo, J.; Kobayashi, T.; Maeda, H.; Yabusaki, Y.; Miyachi, M.; Sakamoto, R.; Nishihara, H. A new method to generate arene-terminated Si(111) and Ge(111) surfaces via a palladium-catalyzed arylation reaction J. Am. Chem. Soc. 2012, 134, 20433-20439
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 20433-20439
    • Yamanoi, Y.1    Sendo, J.2    Kobayashi, T.3    Maeda, H.4    Yabusaki, Y.5    Miyachi, M.6    Sakamoto, R.7    Nishihara, H.8
  • 38
    • 0141818366 scopus 로고    scopus 로고
    • Covalent bond formation to a carbon nanotube metal
    • Kamaras, K.; Itkis, M. E.; Hu, H.; Zhao, B.; Haddon, R. C. Covalent bond formation to a carbon nanotube metal Science 2003, 301, 1501
    • (2003) Science , vol.301 , pp. 1501
    • Kamaras, K.1    Itkis, M.E.2    Hu, H.3    Zhao, B.4    Haddon, R.C.5
  • 39
    • 0344861857 scopus 로고    scopus 로고
    • Sidewall functionalization of single-walled carbon nanotubes by addition of dichlorocarbene
    • Hu, H.; Zhao, B.; Hamon, M. A.; Kamaras, K.; Itkis, M. E.; Haddon, R. C. Sidewall functionalization of single-walled carbon nanotubes by addition of dichlorocarbene J. Am. Chem. Soc. 2003, 125, 14893-14900
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 14893-14900
    • Hu, H.1    Zhao, B.2    Hamon, M.A.3    Kamaras, K.4    Itkis, M.E.5    Haddon, R.C.6
  • 41
    • 0037061512 scopus 로고    scopus 로고
    • 2, and ferrocenium in alcohol solvents
    • 2, and ferrocenium in alcohol solvents J. Phys. Chem. B 2002, 106, 3639-3656
    • (2002) J. Phys. Chem. B , vol.106 , pp. 3639-3656
    • Haber, J.A.1    Lewis, N.S.2
  • 43
    • 57349171432 scopus 로고    scopus 로고
    • Azidation of silicon(111) surfaces
    • Cao, P.; Xu, K.; Heath, J. R. Azidation of silicon(111) surfaces J. Am. Chem. Soc. 2008, 130, 14910-14911
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 14910-14911
    • Cao, P.1    Xu, K.2    Heath, J.R.3
  • 44
    • 36449001216 scopus 로고
    • Infrared spectroscopy study of initial stages of oxidation of hydrogen-terminated Si surfaces stored in air
    • Niwano, M.; Kageyama, J.-i.; Kurita, K.; Kinashi, K.; Takahashi, I.; Miyamoto, N. Infrared spectroscopy study of initial stages of oxidation of hydrogen-terminated Si surfaces stored in air J. Appl. Phys. 1994, 76, 2157-2163
    • (1994) J. Appl. Phys. , vol.76 , pp. 2157-2163
    • Niwano, M.1    Kageyama, J.-I.2    Kurita, K.3    Kinashi, K.4    Takahashi, I.5    Miyamoto, N.6
  • 45
    • 0042493356 scopus 로고    scopus 로고
    • Attenuated total reflection Fourier transform infrared spectroscopy study of the adsorption of organic contaminants on a hydrogen-terminated Si(111) surface in air
    • Ye, S.; Ichihara, T.; Uosaki, K. Attenuated total reflection Fourier transform infrared spectroscopy study of the adsorption of organic contaminants on a hydrogen-terminated Si(111) surface in air Appl. Phys. Lett. 1999, 75, 1562-1564
    • (1999) Appl. Phys. Lett. , vol.75 , pp. 1562-1564
    • Ye, S.1    Ichihara, T.2    Uosaki, K.3
  • 46
    • 0034271246 scopus 로고    scopus 로고
    • Insights into the formation mechanisms of Si-OR monolayers from the thermal reactions of alcohols and aldehydes with Si(111)-H
    • Boukherroub, R.; Morin, S.; Sharpe, P.; Wayner, D. D. M.; Allongue, P. Insights into the formation mechanisms of Si-OR monolayers from the thermal reactions of alcohols and aldehydes with Si(111)-H Langmuir 2000, 16, 7429-7434
    • (2000) Langmuir , vol.16 , pp. 7429-7434
    • Boukherroub, R.1    Morin, S.2    Sharpe, P.3    Wayner, D.D.M.4    Allongue, P.5
  • 48
    • 77957873018 scopus 로고    scopus 로고
    • Thermal and photoinduced covalent attachment of 3-chloro-1-propanol on Si(100)-2×1
    • Shao, Y. X.; Dong, D.; Cai, Y. H.; Wang, S.; Ang, S. G.; Xu, G. Q. Thermal and photoinduced covalent attachment of 3-chloro-1-propanol on Si(100)-2×1 J. Phys. Chem. C 2010, 114, 17159-17165
    • (2010) J. Phys. Chem. C , vol.114 , pp. 17159-17165
    • Shao, Y.X.1    Dong, D.2    Cai, Y.H.3    Wang, S.4    Ang, S.G.5    Xu, G.Q.6
  • 49
    • 84855530248 scopus 로고    scopus 로고
    • Chemical and electrical passivation of Si(111) surfaces
    • Tian, F.; Yang, D.; Opila, R. L.; Teplyakov, A. V. Chemical and electrical passivation of Si(111) surfaces Appl. Surf. Sci. 2012, 258, 3019-3026
    • (2012) Appl. Surf. Sci. , vol.258 , pp. 3019-3026
    • Tian, F.1    Yang, D.2    Opila, R.L.3    Teplyakov, A.V.4
  • 50
    • 33745501203 scopus 로고    scopus 로고
    • Bromine functionalized molecular adlayers on hydrogen passivated silicon surfaces
    • Basu, R.; Kinser, C. R.; Tovar, J. D.; Hersam, M. C. Bromine functionalized molecular adlayers on hydrogen passivated silicon surfaces Chem. Phys. 2006, 326, 144-150
    • (2006) Chem. Phys. , vol.326 , pp. 144-150
    • Basu, R.1    Kinser, C.R.2    Tovar, J.D.3    Hersam, M.C.4
  • 51
    • 0000982459 scopus 로고
    • Tris(trimethylsilyl)silane. A new reducing agent
    • Chatgilialoglu, C.; Griller, D.; Lesage, M. Tris(trimethylsilyl)silane. A new reducing agent J. Org. Chem. 1988, 53, 3641-3642
    • (1988) J. Org. Chem. , vol.53 , pp. 3641-3642
    • Chatgilialoglu, C.1    Griller, D.2    Lesage, M.3
  • 52
    • 33845182970 scopus 로고
    • Rate constants for the reactions of tris(trimethylsilyl)silyl radicals with organic halides
    • Chatgilialoglu, C.; Griller, D.; Lesage, M. Rate constants for the reactions of tris(trimethylsilyl)silyl radicals with organic halides J. Org. Chem. 1989, 54, 2492-2494
    • (1989) J. Org. Chem. , vol.54 , pp. 2492-2494
    • Chatgilialoglu, C.1    Griller, D.2    Lesage, M.3
  • 53
    • 66249095659 scopus 로고    scopus 로고
    • Evidence for initiation of thermal reactions of alkenes with hydrogen-terminated silicon by surface-catalyzed thermal decomposition of the reactant
    • Mischki, T. K.; Lopinski, G. P.; Wayner, D. D. M. Evidence for initiation of thermal reactions of alkenes with hydrogen-terminated silicon by surface-catalyzed thermal decomposition of the reactant Langmuir 2009, 25, 5626-5630
    • (2009) Langmuir , vol.25 , pp. 5626-5630
    • Mischki, T.K.1    Lopinski, G.P.2    Wayner, D.D.M.3
  • 55
    • 34247863738 scopus 로고    scopus 로고
    • Azide-modified graphitic surfaces for covalent attachment of alkyne-terminated molecules by "click" chemistry
    • Devadoss, A.; Chidsey, C. E. D. Azide-modified graphitic surfaces for covalent attachment of alkyne-terminated molecules by "click" chemistry J. Am. Chem. Soc. 2007, 129, 5370-5371
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5370-5371
    • Devadoss, A.1    Chidsey, C.E.D.2
  • 57
    • 57149096043 scopus 로고    scopus 로고
    • Dehydrative cyclocondensation reactions on hydrogen-terminated Si(100) and Si(111): An ex situ tool for the modification of semiconductor surfaces
    • Leftwich, T. R.; Madachik, M. R.; Teplyakov, A. V. Dehydrative cyclocondensation reactions on hydrogen-terminated Si(100) and Si(111): an ex situ tool for the modification of semiconductor surfaces J. Am. Chem. Soc. 2008, 130, 16216-16223
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 16216-16223
    • Leftwich, T.R.1    Madachik, M.R.2    Teplyakov, A.V.3
  • 58
    • 79960629751 scopus 로고    scopus 로고
    • Synthesis of gem-difluorinated cyclopropanes and cyclopropenes: Trifluoromethyltrimethylsilane as a difluorocarbene source
    • Wang, F.; Luo, T.; Hu, J.; Wang, Y.; Krishnan, H. S.; Jog, P. V.; Ganesh, S. K.; Prakash, G. K. S.; Olah, G. A. Synthesis of gem-difluorinated cyclopropanes and cyclopropenes: trifluoromethyltrimethylsilane as a difluorocarbene source Angew. Chem., Int. Ed. 2011, 50, 7153-7157
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 7153-7157
    • Wang, F.1    Luo, T.2    Hu, J.3    Wang, Y.4    Krishnan, H.S.5    Jog, P.V.6    Ganesh, S.K.7    Prakash, G.K.S.8    Olah, G.A.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.