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Volumn , Issue 15, 2009, Pages 1948-1955

Substituent effects on the electronic structure of siloles

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTADIENE DERIVATIVE; SILOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 63849118222     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b822760h     Document Type: Article
Times cited : (155)

References (80)
  • 3
    • 79956060624 scopus 로고    scopus 로고
    • Quantum yields are in many cases much higher in the solid state than in solution; this effect has been referred to as "aggregation-induced emission" and can be understood in terms of suppression in the solid state of internal conversion mechanisms associated with torsions around substituent-silole bonds:
    • H. Murata Z. H. Kafafi M. Uchida Appl. Phys. Lett. 2002 80 189
    • (2002) Appl. Phys. Lett. , vol.80 , pp. 189
    • Murata, H.1    Kafafi, Z.H.2    Uchida, M.3
  • 46
    • 0041538283 scopus 로고    scopus 로고
    • according to the Hartree-Fock calculations of ref. 13 for the case of X = H, the HOMO is intermediate in energy between that of cyclopentadiene and butadiene
    • Y. Yamaguchi Synth. Met. 1996 82 149
    • (1996) Synth. Met. , vol.82 , pp. 149
    • Yamaguchi, Y.1
  • 59
    • 63849175611 scopus 로고    scopus 로고
    • -. However, sometimes it is defined as the negative of this quantity, in which case it is positive number for most organic conjugated species
    • -. However, sometimes it is defined as the negative of this quantity, in which case it is positive number for most organic conjugated species


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.