[Fe(paptH)2] (CF3SO3)2和[Fe(paptH)2] [Fe(CN)5NO] (paptH =双(2-(吡啶-2-基)-4-(吡啶-2-基)噻唑的制备:磁性,Mössbauer和电子光谱性质

Q3 Chemistry
K. Sugiyarto, H. Goodwin
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引用次数: 0

摘要

[Fe(paptH)2][X]的配合物nH2O, (paptH = 2-(吡啶-2-氨基)-4-(吡啶-2-基)-噻唑,X = CF3SO3, n = 1.5, X2 = [Fe(CN)5NO], n = 3)的磁性,Mössbauer和电子光谱性质进行了表征。研究表明,这两种配合物在室温下以五重态为主,而在低温(低于91K)下则以单线态为主。在铁(II)中,这种变化被指定为热自旋态转变,单重态1A1g (LS,低自旋)↔五重态5t2 (HS,高自旋),在实验温度范围内是渐进的、连续的和不完全的,并且在这些情况下没有滞后。这两种配合物在室温(~ 298K)下呈黄褐色,在较低温度下变为红棕色。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation of [Fe(paptH)2] (CF3SO3)2 and [Fe(paptH)2] [Fe(CN)5NO] (paptH = bis(2-(pyridin-2-ylamino)-4-(pyridin-2-yl)thiazole: Magnetic, Mössbauer, and Electronic Spectral Properties
Complexes of [Fe(paptH)2][X]2.nH2O, (paptH = 2-(pyridin-2-ylamino)-4-(pyridin-2-yl)- thiazole, X = CF3SO3 and n = 1.5, and X2 = [Fe(CN)5NO] and n = 3) have been characterized in magnetic, Mössbauer, and electronic spectral properties. The studies reveal that the two complexes are predominantly quintet state at room temperature, but singlet at low temperature (below 91K). The change is assigned as a thermally spin state transition, singlet 1A1g (LS, low-spin) ↔ quintet 5T2g (HS, high-spin), in iron(II), being gradual, continuous, and incomplete at the experimental temperature range, and without hysteresis in these instances. The two complexes were yellowish brown at room temperature (~ 298K) but darkening to reddish brown at the lower temperatures.
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来源期刊
Molekul
Molekul Chemistry-Chemistry (all)
CiteScore
1.30
自引率
0.00%
发文量
31
审稿时长
4 weeks
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