시아노페로센

시아노페로센
시아노페로센 구조식 이미지
카스 번호:
1273-84-3
한글명:
시아노페로센
동의어(한글):
시아노페로센
상품명:
Cyanoferrocene
동의어(영문):
Cyanoferrocene;Ferrocene, cyano-;Ferrocenylnitrile;Ferrocenyl cyanide;Cyclopentadienecarbonitrile, cyclopentadienyliron deriv.
CBNumber:
CB21457014
분자식:
C6H4N.C5H5.Fe
포뮬러 무게:
211.044
MOL 파일:
1273-84-3.mol

시아노페로센 속성

녹는점
107-108℃

안전

시아노페로센 C화학적 특성, 용도, 생산

개요

Cyanoferrocene, [Fe(C5H5)(C6H4N)], forms sheets through hydrogen bonding. The N atom in the molecule accepts hydrogen bonds from C-H bonds in two other molecules, resulting in each molecule being hydrogen-bonded to four others. cyanoferrocene has occupied an important position since it can be converted to a structurally diverse set of ferrocenyl compounds that are attractive synthetic targets due to their chemical and biological properties.

제조 방법

The synthesis of cyanoferrocene involved treating 3.1g (0.01 mol) of iodoferrocene and 3.6g (0.04 mol) of copper(I) cyanide with 20 ml of pyridine, using the same procedure used for preparing chloroferrocene. The resulting crude product was purified by chromatography on Florisil, yielding 1.75 g of cyanoferrocene with a yield of 83%. The melting point of cyanoferrocene was 106-107°C (lit. 107-108°C). A by-product of unidentified yellow crystals was also obtained, weighing 0.15g with a melting point of 157-158°C.

참고 문헌

The Reaction of Haloferrocenes with Copper(Ⅰ) Salts
DOI: 10.1246/bcsj.42.1976
Cyanoferrocene: a Two-Dimensional Network Generated by Short C-H...N Hydrogen Bonds
DOI: 10.1107/S0108270196006233
Efficient one-pot synthesis of cyanoferrocene from ferrocenecarboxaldehyde using NH2OH · HCl/KI/ZnO/CH3CN system
DOI: 10.1016/j.jorganchem.2007.02.002

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