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Volumn 40, Issue 21, 2011, Pages 5643-5658

Polynuclear carbon-rich organometallic complexes: Clarification of the role of the bridging ligand in the redox properties

Author keywords

[No Author keywords available]

Indexed keywords

ANCILLARY LIGANDS; BRIDGING LIGANDS; CARBON RICH; CARBON-RICH ORGANOMETALLICS; EPR SPECTROSCOPY; INTRA-MOLECULAR ELECTRON TRANSFER; METAL DENSITY; METALLIC COMPLEXES; MIXED VALENCE; MIXED-VALENT COMPLEXES; MONOMETALLIC COMPLEX; POLYMETALLIC; QUANTUM-MECHANICAL CALCULATION; REDOX PROCESS; REDOX PROPERTY; REDOX STATE; SPECTROSCOPIC METHOD; THEORETICAL STUDY; THEORETICAL TREATMENTS;

EID: 79955042846     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/c0dt01388a     Document Type: Article
Times cited : (169)

References (156)
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    • Robin and Day's classification established that (1) Class I systems correspond to a trapped valence on one of the two sites; (2) If the 'mixed-valent' atoms are completely undistinguishable the compound is classified as class III with a genuine non-integral valence; (3) Class II lies between the two previous cases with an accessible thermal electron transfer and the presence of an intervalence transfer optical transition, see:
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  • 56
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    • Other parameters should be taken into account as well as temperature dependence, particularly because of vibrational evolution and vibronic coupling, interaction with the electrolyte, ion-pairing possibilities or polarisability effects
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  • 61
    • 5644303218 scopus 로고
    • DFT results were indeed shown to be in good agreement with the experimental spin-densities
    • H. M. McConnell J. Chem. Phys. 1961 35 508. DFT results were indeed shown to be in good agreement with the experimental spin-densities, see ref.
    • (1961) J. Chem. Phys. , vol.35 , pp. 508
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  • 64
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    • The electronic asymmetry resulting from localization of the electron on one side of the oxidized molecule was confirmed through STM images and comparison to theoretical STM images calculated using constrained density-functional theory (CDFT): see ref. 28a
    • Y. Lu R. Quardokus C. S. Lent F. Justaud C. Lapinte S. A. Kandel J. Am. Chem. Soc. 2010 132 13519
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 13519
    • Lu, Y.1    Quardokus, R.2    Lent, C.S.3    Justaud, F.4    Lapinte, C.5    Kandel, S.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.