메뉴 건너뛰기




Volumn 6, Issue , 2015, Pages

1,3,2,5-Diazadiborinine featuring nucleophilic and electrophilic boron centres

Author keywords

[No Author keywords available]

Indexed keywords

1,3,2,5 DIAZADIBORININE DERIVATIVE; BENZENE DERIVATIVE; BORON; CARBON DIOXIDE; PHENYLACETYLENE; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

EID: 84931275240     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms8340     Document Type: Article
Times cited : (80)

References (41)
  • 1
    • 0002530663 scopus 로고
    • Sur la constitution des substances aromatiques
    • Kekulé, A. Sur la constitution des substances aromatiques. Bull. Soc. Chim. Fr 3, 98-110 (1865).
    • (1865) Bull. Soc. Chim. Fr , vol.3 , pp. 98-110
    • Kekulé, A.1
  • 2
    • 0002197464 scopus 로고
    • On new compounds of carbon and hydrogen, and on certain other products obtained during the decomposition of oil by heat
    • Faraday, M. On new compounds of carbon and hydrogen, and on certain other products obtained during the decomposition of oil by heat. Phil. Trans. R. Soc. Lond. 115, 440-466 (1825).
    • (1825) Phil. Trans. R. Soc. Lond. , vol.115 , pp. 440-466
    • Faraday, M.1
  • 4
    • 81555200676 scopus 로고    scopus 로고
    • Effect on ring current of the Kekulé vibration in aromatic and antiaromatic rings
    • Bean, D. E. & Fowler, P. W. Effect on ring current of the Kekulé vibration in aromatic and antiaromatic rings. J. Phys. Chem. A 115, 13649-13656 (2011).
    • (2011) J. Phys. Chem. A , vol.115 , pp. 13649-13656
    • Bean, D.E.1    Fowler, P.W.2
  • 5
    • 77950843909 scopus 로고    scopus 로고
    • Is delocalization a prerequisite for stability of ring systems? A case study of some inorganic rings
    • Phukan, A. K., Guha, A. K. & Silvi, B. Is delocalization a prerequisite for stability of ring systems? A case study of some inorganic rings. Dalton Trans. 39, 4126-4137 (2010).
    • (2010) Dalton Trans. , vol.39 , pp. 4126-4137
    • Phukan, A.K.1    Guha, A.K.2    Silvi, B.3
  • 6
    • 38049038327 scopus 로고    scopus 로고
    • B-N versus C-C: How similar are they?
    • Liu, Z. & Marder, T. B. B-N versus C-C: how similar are they? Angew. Chem. Int. Ed. 47, 242-244 (2008).
    • (2008) Angew Chem. Int. Ed. , vol.47 , pp. 242-244
    • Liu, Z.1    Marder, T.B.2
  • 7
    • 66149186390 scopus 로고    scopus 로고
    • B-N as a C-C substitute in aromatic systems
    • Bosdet, M. J. D. & Piers, W. E. B-N as a C-C substitute in aromatic systems. Can. J. Chem. 87, 8-29 (2009).
    • (2009) Can. J. Chem. , vol.87 , pp. 8-29
    • Bosdet, M.J.D.1    Piers, W.E.2
  • 8
    • 68149161075 scopus 로고    scopus 로고
    • Aromatic borataheterocycles: Surrogates for cyclopentadienyl in transition-metal complexes
    • Ashe, III A. J. Aromatic borataheterocycles: surrogates for cyclopentadienyl in transition-metal complexes. Organometallics 28, 4236-4248 (2009).
    • (2009) Organometallics , vol.28 , pp. 4236-4248
    • Ashe, A.J.1
  • 9
    • 37049060355 scopus 로고
    • New heteroaromatic compounds. Part I. 9-Aza-10-boraphenanthrene
    • Dewar, M. J. S., Kubba, V. P. & Pettit, R. New heteroaromatic compounds. Part I. 9-Aza-10-boraphenanthrene. J. Chem. Soc. 3073-3076 (1958).
    • (1958) J. Chem. Soc. , pp. 3073-3076
    • Dewar, M.J.S.1    Kubba, V.P.2    Pettit, R.3
  • 11
    • 33747784612 scopus 로고    scopus 로고
    • Triphenylene analogues with B2N2C2 cores: Synthesis, structure, redox behavior, and photophysical properties
    • Jaska, C. A. et al. Triphenylene analogues with B2N2C2 cores: synthesis, structure, redox behavior, and photophysical properties. J. Am. Chem. Soc. 128, 10885-10896 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 10885-10896
    • Jaska, C.A.1
  • 12
    • 33749234189 scopus 로고    scopus 로고
    • A s-donor with a planar six-p-electron B2N2C2 framework: Anionic N-heterocyclic carbene or heterocyclic terphenyl anion?
    • Forster, T. D. et al. A s-donor with a planar six-p-electron B2N2C2 framework: anionic N-heterocyclic carbene or heterocyclic terphenyl anion? Angew. Chem. Int. Ed. 45, 6356-6359 (2006).
    • (2006) Angew Chem. Int. Ed. , vol.45 , pp. 6356-6359
    • Forster, T.D.1
  • 13
    • 79960948962 scopus 로고    scopus 로고
    • Synthesis and characterization of a neutral tricoordinate organoboron isoelectronic with amines
    • Kinjo, R., Donnadieu, B., Celik, M. A., Frenking, G. & Bertrand, G. Synthesis and characterization of a neutral tricoordinate organoboron isoelectronic with amines. Science 333, 610-613 (2011).
    • (2011) Science , vol.333 , pp. 610-613
    • Kinjo, R.1    Donnadieu, B.2    Celik, M.A.3    Frenking, G.4    Bertrand, G.5
  • 14
    • 84906785892 scopus 로고    scopus 로고
    • Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile
    • Kong, L., Li, Y., Ganguly, R., Vidovic, D. & Kinjo, R. Isolation of a bis(oxazol-2-ylidene)-phenylborylene adduct and its reactivity as a boron-centered nucleophile. Angew. Chem. Int. Ed. 53, 9280-9283 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 9280-9283
    • Kong, L.1    Li, Y.2    Ganguly, R.3    Vidovic, D.4    Kinjo, R.5
  • 15
    • 84903148332 scopus 로고    scopus 로고
    • An efficient synthetic route to stable bis(carbene)borylenes [(L1)(L2)BH]
    • Ruiz, D. A., Melaimi, M. & Bertrand, G. An efficient synthetic route to stable bis(carbene)borylenes [(L1)(L2)BH]. Chem. Commun. 50, 7837-7839 (2014).
    • (2014) Chem. Commun. , vol.50 , pp. 7837-7839
    • Ruiz, D.A.1    Melaimi, M.2    Bertrand, G.3
  • 16
    • 84928139723 scopus 로고    scopus 로고
    • Diverse reactivity of a tricoordinate organoboron L2PhB: (L=oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
    • Kong, L., Ganguly, R., Li, Y. & Kinjo, R. Diverse reactivity of a tricoordinate organoboron L2PhB: (L=oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors. Chem. Sci. 6, 2893-2902 (2015).
    • (2015) Chem. Sci. , vol.6 , pp. 2893-2902
    • Kong, L.1    Ganguly, R.2    Li, Y.3    Kinjo, R.4
  • 17
    • 33845202046 scopus 로고
    • Direct approach to measuring the Franck-Condon barrier to electron transfer between metal ions
    • Creutz, C. & Taube, H. Direct approach to measuring the Franck-Condon barrier to electron transfer between metal ions. J. Am. Chem. Soc. 91, 3988-3989 (1969).
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 3988-3989
    • Creutz, C.1    Taube, H.2
  • 18
    • 33845228938 scopus 로고
    • Binuclear complexes of ruthenium ammines
    • Creutz, C. & Taube, H. Binuclear complexes of ruthenium ammines. J. Am. Chem. Soc. 95, 1086-1094 (1973).
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 1086-1094
    • Creutz, C.1    Taube, H.2
  • 19
    • 77957027443 scopus 로고
    • Mixed-valence chemistry: A survey and classification
    • Robin, M. B. & Day, P. Mixed-valence chemistry: a survey and classification. Adv. Inorg. Chem. Radiochem 10, 247-422 (1967).
    • (1967) Adv. Inorg. Chem. Radiochem , vol.10 , pp. 247-422
    • Robin, M.B.1    Day, P.2
  • 20
    • 77955677886 scopus 로고    scopus 로고
    • Electronic communication through unsaturated hydrocarbon bridges in homobimetallic organometallic complexes
    • Aguirre-Etcheverry, P. & O'Hare, D. Electronic communication through unsaturated hydrocarbon bridges in homobimetallic organometallic complexes. Chem. Rev. 110, 4839-4864 (2010).
    • (2010) Chem. Rev. , vol.110 , pp. 4839-4864
    • Aguirre-Etcheverry, P.1    O'hare, D.2
  • 21
    • 80051771818 scopus 로고    scopus 로고
    • Organic mixed valence
    • Hankache, J. & Wenger, O. S. Organic mixed valence. Chem. Rev. 111, 5138-5178 (2011).
    • (2011) Chem. Rev. , vol.111 , pp. 5138-5178
    • Hankache, J.1    Wenger, O.S.2
  • 22
    • 84884240304 scopus 로고    scopus 로고
    • Diradicals
    • Abe, M. Diradicals. Chem. Rev. 113, 7011-7088 (2013).
    • (2013) Chem. Rev. , vol.113 , pp. 7011-7088
    • Abe, M.1
  • 23
    • 84855453111 scopus 로고    scopus 로고
    • Organic mixed-valence compounds: A playground for electrons and holes
    • Heckmann, A. & Lambert, C. Organic mixed-valence compounds: a playground for electrons and holes. Angew. Chem. Int. Ed. 51, 326-392 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 326-392
    • Heckmann, A.1    Lambert, C.2
  • 24
    • 84875055802 scopus 로고    scopus 로고
    • Twists and turns: Studies of the complexes and properties of bimetallic complexes featuring phenylene ethynylene and related bridging ligands
    • Low, P. J. Twists and turns: studies of the complexes and properties of bimetallic complexes featuring phenylene ethynylene and related bridging ligands. Coord. Chem. Rev. 257, 1507-1532 (2013).
    • (2013) Coord. Chem. Rev. , vol.257 , pp. 1507-1532
    • Low, P.J.1
  • 25
    • 84903289430 scopus 로고    scopus 로고
    • Quantum-chemical insights into mixed-valence systems: Within and beyond the Robin-Day scheme
    • Parthey, M. & Kaupp, M. Quantum-chemical insights into mixed-valence systems: within and beyond the Robin-Day scheme. Chem. Soc. Rev. 43, 5067-5088 (2014).
    • (2014) Chem. Soc. Rev. , vol.43 , pp. 5067-5088
    • Parthey, M.1    Kaupp, M.2
  • 27
    • 0032571485 scopus 로고    scopus 로고
    • Isolation of a benzene valence isomer with one-electron phosphorus-phosphorus bonds
    • Canac, Y. et al. Isolation of a benzene valence isomer with one-electron phosphorus-phosphorus bonds. Science 279, 2080-2082 (1998).
    • (1998) Science , vol.279 , pp. 2080-2082
    • Canac, Y.1
  • 28
    • 0005376891 scopus 로고    scopus 로고
    • Dual excimer emission of p-terphenyl induced by g-cyclodextrin in aqueous solutions
    • Pistolis, G. Dual excimer emission of p-terphenyl induced by g-cyclodextrin in aqueous solutions. Chem. Phys. Lett. 304, 371-377 (1999).
    • (1999) Chem. Phys. Lett. , vol.304 , pp. 371-377
    • Pistolis, G.1
  • 29
    • 80055006049 scopus 로고    scopus 로고
    • Aggregation-induced emission
    • Hong, Y., Lam, J. W. Y. & Tang, B. Z. Aggregation-induced emission. Chem. Soc. Rev. 40, 5361-5388 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 5361-5388
    • Hong, Y.1    Lam, J.W.Y.2    Tang, B.Z.3
  • 30
    • 68749120723 scopus 로고    scopus 로고
    • Aggregation-induced emission: Phenomenon, mechanism and applications
    • Hong, Y., Lam, J. W. Y. & Tang, B. Z. Aggregation-induced emission: phenomenon, mechanism and applications. Chem. Commun. 45, 4332-4353 (2009).
    • (2009) Chem. Commun. , vol.45 , pp. 4332-4353
    • Hong, Y.1    Lam, J.W.Y.2    Tang, B.Z.3
  • 31
    • 84880127094 scopus 로고    scopus 로고
    • Boronsubstituted 1,3-dihydro-1,3-azaborines: Synthesis, structure, and evaluation of aromaticity
    • Xu, S., Mikulas, T. C., Zakharov, L. N., Dixon, D. A. & Liu, S.-Y. Boronsubstituted 1,3-dihydro-1,3-azaborines: synthesis, structure, and evaluation of aromaticity. Angew. Chem. Int. Ed. 52, 7527-7531 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 7527-7531
    • Xu, S.1    Mikulas, T.C.2    Zakharov, L.N.3    Dixon, D.A.4    Liu, S.-Y.5
  • 33
    • 73349126734 scopus 로고    scopus 로고
    • Frustrated Lewis pairs: Metal-free hydrogen activation and more
    • Stephan, D. W. & Erker, G. Frustrated Lewis pairs: metal-free hydrogen activation and more. Angew. Chem. Int. Ed. 49, 46-76 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 46-76
    • Stephan, D.W.1    Erker, G.2
  • 34
    • 74749089263 scopus 로고    scopus 로고
    • Main-group elements as transition metals
    • Power, P. P. Main-group elements as transition metals. Nature 463, 171-177 (2010).
    • (2010) Nature , vol.463 , pp. 171-177
    • Power, P.P.1
  • 35
    • 79953673603 scopus 로고    scopus 로고
    • Zwitterionic and donor-stabilized N-heterocyclic silylenes (NHSis) for metal-free activation of small molecules
    • Yao, S., Xiong, Y. & Driess, M. Zwitterionic and donor-stabilized N-heterocyclic silylenes (NHSis) for metal-free activation of small molecules. Organometallics 30, 1748-1767 (2011).
    • (2011) Organometallics , vol.30 , pp. 1748-1767
    • Yao, S.1    Xiong, Y.2    Driess, M.3
  • 36
    • 84860346860 scopus 로고    scopus 로고
    • Group 14 hydrides with low valent elements for activation of small molecules
    • Mandal, S. K. & Roesky, H. W. Group 14 hydrides with low valent elements for activation of small molecules. Acc. Chem. Res. 45, 298-307 (2012).
    • (2012) Acc. Chem. Res. , vol.45 , pp. 298-307
    • Mandal, S.K.1    Roesky, H.W.2
  • 37
    • 84923094674 scopus 로고    scopus 로고
    • Frustrated Lewis pairs: From concept to catalysis
    • Stephan, D. W. Frustrated Lewis pairs: from concept to catalysis. Acc. Chem. Res. 48, 306-316 (2015).
    • (2015) Acc. Chem. Res. , vol.48 , pp. 306-316
    • Stephan, D.W.1
  • 38
    • 0010549034 scopus 로고
    • Bis-(polyfluoroalkyl)-acetylenes. II. Bicycloöctatrienes through 1,4-addition of bis-(polyfluoroalkyl)-acetylenes to aromatic rings
    • Krespan, C. G., McKusick, B. C. & Cairns, T. L. Bis-(polyfluoroalkyl)-acetylenes. II. Bicycloöctatrienes through 1,4-addition of bis-(polyfluoroalkyl)-acetylenes to aromatic rings. J. Am. Chem. Soc. 83, 3428-3432 (1961).
    • (1961) J. Am. Chem. Soc. , vol.83 , pp. 3428-3432
    • Krespan, C.G.1    McKusick, B.C.2    Cairns, T.L.3
  • 39
    • 0004965279 scopus 로고
    • Synthesis and physical properties of barrelene, a unique Moebius-like molecule
    • Zimmerman, H. E., Grunewald, G. L., Paufler, R. M. & Sherwin, M. A. Synthesis and physical properties of barrelene, a unique Moebius-like molecule. J. Am. Chem. Soc. 91, 2330-2338 (1969).
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 2330-2338
    • Zimmerman, H.E.1    Grunewald, G.L.2    Paufler, R.M.3    Sherwin, M.A.4
  • 40
    • 84901838643 scopus 로고    scopus 로고
    • Frustrated Lewis pair chemistry of carbon, nitrogen and sulfur oxides
    • Stephan, D. W. & Erker, G. Frustrated Lewis pair chemistry of carbon, nitrogen and sulfur oxides. Chem. Sci. 5, 2625-2641 (2014).
    • (2014) Chem. Sci. , vol.5 , pp. 2625-2641
    • Stephan, D.W.1    Erker, G.2
  • 41
    • 0037174408 scopus 로고    scopus 로고
    • Efficient chemoselective carboxylation of aromatics to arylcarboxylic acids with a superelectrophilically activated carbon dioxide-Al2Cl6/Al System
    • Olah, G. A. et al. Efficient chemoselective carboxylation of aromatics to arylcarboxylic acids with a superelectrophilically activated carbon dioxide-Al2Cl6/Al System. J. Am. Chem. Soc. 124, 11379-11391 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11379-11391
    • Olah, G.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.