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Volumn 119, Issue 45, 1997, Pages 10976-10986

Highly strained, ring-tilted [1]ferrocenophanes containing group 16 elements in the bridge: Synthesis, structures, and ring-opening oligomerization and polymerization of [1]thia- and [1]selenaferrocenophanes

Author keywords

[No Author keywords available]

Indexed keywords

FERROCENE DERIVATIVE; SELENIUM DERIVATIVE;

EID: 0030723096     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja972043u     Document Type: Article
Times cited : (122)

References (74)
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    • Single-bond covalent radii (Si, 1.17 Å; P, 1.12 Å; S 1.02 Å) and covalent single-bond distances (Si-C, 1.87 Å; P-C, 1.84 Å; S-C, 1.82 A) suggest that sulfur would represent the smallest element incorporated into the bridge of a [1]ferrocenophane. See: Jolly, W. L. The Principles of Inorganic Chemistry; McGraw-Hill: New York, 1976; Chapter 2.
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    • note
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    • Single-bond covalent radii (Ge, 1.22; As, 1.22 Å; Se, 1.17 Å). See ref 39
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    • note
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    • note
    • It has, however, been shown for several poly(ferrocenylsilanes) that GPC underestimates the true molecular weight by ca. 30%. See refs 20a and b.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.