메뉴 건너뛰기




Volumn 122, Issue 36, 2000, Pages 8797-8798

Discovery of the first metallaquinone [11]

Author keywords

[No Author keywords available]

Indexed keywords

AMPHOLYTE; METALLAQUINONE DERIVATIVE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034644410     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja001759d     Document Type: Letter
Times cited : (59)

References (35)
  • 1
    • 0343676508 scopus 로고
    • Wiley: London
    • The Chemistry of the Quinoid Compounds, Parts 1 and 2; Patai, S., Ed.; Wiley: London, 1974; The Chemistry of the Quinoid Compounds, Parts 1 and 2; Patai, S., Rappoport, Z., Eds.; Wiley: Chichester, 1988.
    • (1974) The Chemistry of the Quinoid Compounds , Issue.1-2 PARTS
    • Patai, S.1
  • 2
    • 0003829752 scopus 로고
    • Wiley: Chichester
    • The Chemistry of the Quinoid Compounds, Parts 1 and 2; Patai, S., Ed.; Wiley: London, 1974; The Chemistry of the Quinoid Compounds, Parts 1 and 2; Patai, S., Rappoport, Z., Eds.; Wiley: Chichester, 1988.
    • (1988) The Chemistry of the Quinoid Compounds , Issue.1-2 PARTS
    • Patai, S.1    Rappoport, Z.2
  • 21
    • 0342371345 scopus 로고    scopus 로고
    • note
    • -1, are very similar to those for 4a (see above).
  • 23
    • 0342371346 scopus 로고    scopus 로고
    • note
    • Relevant distances (Å) and angles (deg): 4b: Ru(1)-C(11) 2.121-(6); O(1)-C(14) 1.373(8); C(11)-C(12) 1.396(9); C(11)-C(16) 1.397(9); C(12)-C(13) 1.386(9); C(13)-C(14) 1.372(9); C(14)-C(15) 1.393(10); C(15)-C(16) 1.410(9); P(2)-Ru(1)-P(3) 157.46(6); C(2)-Ru(1)-C(3) 99.1-(3). 3a: Ru(1)-C(11) 2.117(3); O(1)-C(14) 1.370(4); C(11)-C(12) 1.410-(4); C(11)-C(16) 1.398(4); C(12)-C(13) 1.387(5); C(13)-C(14) 1.380(5); C(14)-C(15) 1.392(4); C(15)-C(16) 1.392(5); P(2)-Ru(1)-P(3) 157.50-(3); C(5)-Ru(1)-C(6) 92.91(14).
  • 28
    • 0033515394 scopus 로고    scopus 로고
    • and references therein
    • Dapprich, S.; Komaromi, I.; Byun, K. S.; Morokuma, K.; Frisch, M. J. J. Mol. Struct. (THEOCHEM) 1999, 461, 1 and references therein. The inner layer corresponds essentially to the R = H model compound; effects of the outer layer (i.e., R = t-Bu) were considered to be mostly sterical, and hence HF/LANL1MB was considered sufficient there.
    • (1999) J. Mol. Struct. (THEOCHEM) , vol.461 , pp. 1
    • Dapprich, S.1    Komaromi, I.2    Byun, K.S.3    Morokuma, K.4    Frisch, M.J.5
  • 34
    • 0032533083 scopus 로고    scopus 로고
    • (b) Stratmann, R. E.; Scuseria, G. E.; Frisch, M. J. J. Chem. Phys. 1998, 109, 8218. The calculations were carried out using the B3LYP functional with the LANL2DZP+ basis set, diffuse function exponents having been taken from Clark, T.; Chandrasekhar, J.; Spitznagel, G. W.; von Ragué Schleyer, P. J. Comput. Chem. 1983, 4, 294.
    • (1998) J. Chem. Phys. , vol.109 , pp. 8218
    • Stratmann, R.E.1    Scuseria, G.E.2    Frisch, M.J.3
  • 35
    • 84986468715 scopus 로고
    • (b) Stratmann, R. E.; Scuseria, G. E.; Frisch, M. J. J. Chem. Phys. 1998, 109, 8218. The calculations were carried out using the B3LYP functional with the LANL2DZP+ basis set, diffuse function exponents having been taken from Clark, T.; Chandrasekhar, J.; Spitznagel, G. W.; von Ragué Schleyer, P. J. Comput. Chem. 1983, 4, 294.
    • (1983) J. Comput. Chem. , vol.4 , pp. 294
    • Clark, T.1    Chandrasekhar, J.2    Spitznagel, G.W.3    Von Ragué Schleyer, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.