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Volumn 14, Issue 6, 2014, Pages 2697-2702

Naming interactions from the electrophilic site

Author keywords

[No Author keywords available]

Indexed keywords

IONS;

EID: 84901919637     PISSN: 15287483     EISSN: 15287505     Source Type: Journal    
DOI: 10.1021/cg5001717     Document Type: Article
Times cited : (192)

References (75)
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    • Pure Appl. Chem. 2011, 83, 1619-1636.
    • (2011) Pure Appl. Chem. , vol.83 , pp. 1619-1636
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    • 85050577234 scopus 로고    scopus 로고
    • Kemsley, J. Chem. Eng. News 2014, 92 (6 January) 25-26
    • (2014) Chem. Eng. News , vol.92 , Issue.6 JAN. , pp. 25-26
    • Kemsley, J.1
  • 68
    • 0000679279 scopus 로고
    • We are listing below Refcodes, and the corresponding references, of some structures reported in the CSD where the observed contacts formed by aluminium, gallium, indium, and thallium are consistent with an electrophilic behaviour of these elements. BATLEN
    • We are listing below Refcodes, and the corresponding references, of some structures reported in the CSD where the observed contacts formed by aluminium, gallium, indium, and thallium are consistent with an electrophilic behaviour of these elements. BATLEN: Atwood, J. L.; Hrncir, D. C.; Rogers, R. D.; Howard, J. A. K. J. Am. Chem. Soc. 1981, 103, 6787-6788
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 6787-6788
    • Atwood, J.L.1    Hrncir, D.C.2    Rogers, R.D.3    Howard, J.A.K.4
  • 73
    • 84866140066 scopus 로고    scopus 로고
    • wherein the C-Li bond is remarkably longer than the Li-O bond (224.5 pm versus 197.9 pm). A similar situation is observed in the ethyl ether solvate
    • Langer, J.; Köhler, M.; Fischer, R.; Dündar, F.; Görls, H.; Westerhausen, M. Organometallics 2012, 31, 6172-6182 wherein the C-Li bond is remarkably longer than the Li-O bond (224.5 pm versus 197.9 pm). A similar situation is observed in the ethyl ether solvate
    • (2012) Organometallics , vol.31 , pp. 6172-6182
    • Langer, J.1    Köhler, M.2    Fischer, R.3    Dündar, F.4    Görls, H.5    Westerhausen, M.6
  • 74
    • 0020798850 scopus 로고
    • several other analogous systems, e.g. ENAWOF
    • Hope, H.; Power, P. P. J. Am. Chem. Soc. 1982, 105, 5320-5324 and several other analogous systems, e.g., ENAWOF
    • (1982) J. Am. Chem. Soc. , vol.105 , pp. 5320-5324
    • Hope, H.1    Power, P.P.2
  • 75
    • 0141605074 scopus 로고    scopus 로고
    • Even more remarkable, two or three lithium atoms are bound to a single benzene carbon in these solvates. The robustness of the proposed generalization is confirmed by the fact that whatever "bond" is considered the "interaction", lithium is the electrophilic ending, and the interaction is realistically designated a lithium bond
    • Vestergren, M.; Eriksson, J.; Hilmersson, G.; Hakansson, M. J. Organomet. Chem. 2003, 682, 172-179 Even more remarkable, two or three lithium atoms are bound to a single benzene carbon in these solvates. The robustness of the proposed generalization is confirmed by the fact that whatever "bond" is considered the "interaction", lithium is the electrophilic ending, and the interaction is realistically designated a lithium bond
    • (2003) J. Organomet. Chem. , vol.682 , pp. 172-179
    • Vestergren, M.1    Eriksson, J.2    Hilmersson, G.3    Hakansson, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.