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首页> 外文期刊>Inorganica Chimica Acta >Polymorphism in dinuclear Cu(II) compounds-polymorphism caused by different degrees of hydration: the structures of [Cu(HL)](2)Cl(2)4H(2)O (I), [Cu(HL)](2)Cl-2 center dot 2H(2)O (II), [Cu(HL)](2))(NO3)(2)center dot 4H(2)O (III), [Cu(HL)](2))(NO3)(2)c
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Polymorphism in dinuclear Cu(II) compounds-polymorphism caused by different degrees of hydration: the structures of [Cu(HL)](2)Cl(2)4H(2)O (I), [Cu(HL)](2)Cl-2 center dot 2H(2)O (II), [Cu(HL)](2))(NO3)(2)center dot 4H(2)O (III), [Cu(HL)](2))(NO3)(2)c

机译:双核Cu(II)化合物的多态性-不同水化程度引起的多态性:[Cu(HL)](2)Cl(2)4H(2)O(I),[Cu(HL)](2 )Cl-2中心点2H(2)O(II),[Cu(HL)](2))(NO3)(2)中心点4H(2)O(III),[Cu(HL)](2 ))(NO3)(2)c

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摘要

Compounds of composition [CiuHL)](2)Cl-2 (.) 4H(2)O (I), [Cu(HL)](2)Cl-2H(2)O (II), [Cu(HL)](2))(NO3)(2) (.) 4H(2)O (III), [Cu(HL)](2))(NO3)(2) (.) 2H(2)O (IV) and [Cu(HL)](2))(ClO4)(2) (.) 2H(2)O (V) (HL = [(3-aminopropyl)-di-(2-hydroxopropyl)]-amine anion) were prepared and their crystal structures determined. Compounds I. IV and V crystallize in the same space group, P2(1)/(n), and are very close to being isomorphous and isostructural. II Crystallizes in space group Peab, while III crystallizes in C21c. The pairs of compounds I-II and III-IV are examples of hydration polymorphism. Efforts to obtain polymorphic forms of V have, thus far, been negative. All five compounds contain a central bi-metallic core consisting of two Cu(II) cations bridged by two oxygens. The resulting species are antiferromagnetically coupled and can nicely be fitted to a Bleany-Bowers model with great precision. Electron spin resonance studies were carried out in solid powders and in frozen solutions, at 77 K in both instances. The g-factors obtained from the latter studies were used in the fitting of the magnetism measurements, which were made between 5 and 295 K. Counter anions were changed on purpose in order to ascertain the manner in which counter ions exert ail effect in the selection of the crystallization pathway chosen. Also, solvent changes were made which resulted in the polymorphism observed, and which was due to variations in the ratios of the solvent components (e.g., methanol-water). All five cations contain one Cu(II)-OH2 bond: and. the length of this bond is the primary difference in the stereochemistry of the cations. They range from 2.731 to 3.959 Angstrom. A discussion is given of the arguments for and against considering the two longest distances (3.827 and 3.959 Angstrom) as true bonds. (C) 2003 Elsevier B.V. All rights reserved. [References: 37]
机译:组成为[CiuHL]] [2)Cl-2(。)4H(2)O(I),[Cu(HL)](2)Cl-2H(2)O(II),[Cu(HL) ](2))(NO3)(2)(。)4H(2)O(III),[Cu(HL)](2))(NO3)(2)(。)2H(2)O(IV)和[Cu(HL)](2))(ClO4)(2)(。)2H(2)O(V)(HL = [(3-氨基丙基)-二-(2-羟丙基)]-胺阴离子)制备并确定其晶体结构。化合物I. IV和V在相同的空间群P2(1)/(n)中结晶,并且非常接近同构和同构。 II在Peab空间群中结晶,而III在C21c中结晶。化合物I-II和III-IV对是水合多态性的实例。迄今为止,获得V的多晶型形式的努力是负面的。所有这五个化合物都包含一个中心双金属核,该核心由两个由两个氧桥接的Cu(II)阳离子组成。产生的物质是反铁磁耦合的,可以很好地拟合到Bleany-Bowers模型。在两种情况下,固体粉末和冷冻溶液中的电子自旋共振研究均在77 K下进行。从后来的研究中获得的g因子用于进行5至295 K之间的磁性测量的拟合。故意改变抗衡阴离子,以确定抗衡离子在选择中发挥全部作用的方式选择的结晶途径。而且,进行溶剂改变,这导致观察到多态性,这是由于溶剂组分(例如,甲醇-水)的比例变化而引起的。所有五个阳离子均包含一个Cu(II)-OH2键:和。该键的长度是阳离子立体化学的主要区别。它们的范围从2.731到3.959埃。讨论了赞成和反对将两个最长距离(3.827和3.959埃)视为真实键的论点。 (C)2003 Elsevier B.V.保留所有权利。 [参考:37]

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