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Volumn 71, Issue 11, 1998, Pages 2621-2627

Solvatochromism and structure of acetylacetonatocopper(II) complexes with N,N'-dipropyl-,N,N,N',N'-tetrapropyl-, and N,N- and N,N'- diisopropylethylenediamines

Author keywords

[No Author keywords available]

Indexed keywords

COPPER COMPLEX; ETHYLENEDIAMINE DERIVATIVE;

EID: 0031763514     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.71.2621     Document Type: Article
Times cited : (18)

References (24)
  • 1
    • 0002692230 scopus 로고
    • ed by G. Wilkinson, R. D. Gillard, and J. A. McCleverty, Pergamon, Oxford
    • Cf. D. A. House, "Comprehensive Coordination Chemistry," ed by G. Wilkinson, R. D. Gillard, and J. A. McCleverty, Pergamon, Oxford (1987), Vol. 2, p. 23 ff.
    • (1987) Comprehensive Coordination Chemistry , vol.2
    • House, D.A.1
  • 6
    • 85038551816 scopus 로고
    • B. S. Thesis, Josai University, Japan
    • 2O and u-dipen in methanol. Cf. T. Masutani, B. S. Thesis, Josai University, Japan, 1995.
    • (1995)
    • Masutani, T.1
  • 8
  • 12
    • 85038554143 scopus 로고    scopus 로고
    • note
    • This is because (i) bulky N-isopropyl groups are expected to be more sterically active than N-propyl groups, and (ii) N-alkyl groups in s-complexes of en derivatives usually tend to occupy equatorial positions with respect to the chelate ring, in u-dipen, however, one such group is forced to occupy an axial position, increasing axial steric hindrance (cf. Ref. 1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.