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Volumn 131, Issue 22, 2009, Pages 7817-7827

Exceptional sensitivity of metal-aryl bond energies to ortho-fluorine substituents: Influence of the metal, the coordination sphere, and the spectator ligands on M-C/H-C bond energy correlations

Author keywords

[No Author keywords available]

Indexed keywords

ARYL RINGS; BOND ENERGIES; C-H OXIDATIVE; COORDINATION SPHERE; DFT CALCULATION; FLUORINE SUBSTITUENTS; FLUORINE SUBSTITUTION; IONICITY; LINEAR FUNCTIONS; METAL FRAGMENTS; PERIODIC TABLE; SPECTATOR LIGANDS;

EID: 67650531384     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja901640m     Document Type: Article
Times cited : (169)

References (81)
  • 8
    • 84886565004 scopus 로고    scopus 로고
    • Advances in Carbon-Hydrogen Activation
    • Crabtree, R. H., Mingos, D. M. P., Eds.; Elsevier: Amsterdam, Chapter 25
    • (c) Jones, W. D. Advances in Carbon-Hydrogen Activation. In Comprehensive Organometallic Chemistry III; Crabtree, R. H., Mingos, D. M. P., Eds.; Elsevier: Amsterdam, 2006; Vol.1 Chapter 25, p 699.
    • (2006) Comprehensive Organometallic Chemistry III , vol.1 , pp. 699
    • Jones, W.D.1
  • 57
    • 67650552365 scopus 로고    scopus 로고
    • The calculated energies for proton dissociation were as follows: C6H6, 1782.5 kJ mol-1; C6FH5, 1729.8 kJ mol-1; 1,3-C6F2H4, 1677.1 kJ mol-1. In the two last cases, the negative charge lies in the 1-position with fluorine in the 2-position and the 2,6-positions, respectively
    • The calculated energies for proton dissociation were as follows: C6H6, 1782.5 kJ mol-1; C6FH5, 1729.8 kJ mol-1; 1,3-C6F2H4, 1677.1 kJ mol-1. In the two last cases, the negative charge lies in the 1-position with fluorine in the 2-position and the 2,6-positions, respectively.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.