首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis and examination of amine-cyanocarboxyboranes, the boron analogues of alpha-cyanocarboxylic acids: X-ray structural study of the first lactam containing a boron atom in the lactam ring
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Synthesis and examination of amine-cyanocarboxyboranes, the boron analogues of alpha-cyanocarboxylic acids: X-ray structural study of the first lactam containing a boron atom in the lactam ring

机译:胺-氰基羧基硼烷(α-氰基羧酸的硼类似物)的合成和检查:内酰胺环中第一个含硼原子的内酰胺的X射线结构研究

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摘要

The first representatives of chiral boron atom-containing amine-cyanomethoxycarbonyl boranes (A . BH(CN)COOMe) have been synthesized either from the corresponding amine-bromocyanomethoxycarbonylborane complexes with [BU4N]CN or from Me3N.BH(CN)COOMe and an amine in a base-exchange reaction. Acid hydrolyses of methyl esters generated the free acids (A.BH(CN)COOH), which are isoelectronic to the alpha-cyano carboxylic acids. Their pK(a) values and hydrolysis half-lives in acidic medium (that is rate of proton reduction) have been determined. Similarly to the alpha cyano carboxylic acids, the cyano group attached to the boron (in alpha position to the COOH group) increased the acid strength of carboxy boranes with 2.0-2.5 orders of magnitude. Independently from the type of the amine, pK(a) values of the amine-cyanocarboxyhoranes (6.34-5.82) decrease consistently with the increase of pK(b) values of the amines. Hydrolytic decomposition rate of the alkylamine complexes increases with increasing pKb values of the amines while the opposite was found for pyridine base complexes. When considering both types of the amines, hydrolysis half-lives of the complexes range over several orders of magnitude from 0.005 to 400 h. Based on these observations protonation of the amine nitrogen atom appears to be the rate determining step in the hydrolysis process. With loss of methanol, 2-NH2-py.BH(CN)COOMe transformed into a five membered lactam derivative. X-ray diffraction revealed that the pyridine ring is coplanar with the five membered lactam ring. In the crystal two molecules are connected in a head to tail arrangement by strong intermolecular H-bonds between N(2)-H and the carbonyl oxygen (01) with a donor and acceptor distance of 2.867(3) A. Three new cyanomethoxycarbonylborates having the composition of K[BHn(CN)(3-n)COOMe] (n = 1, 2) and K[B(OH)(CN)(2-) COOMe] have also been synthesized and their properties examined. (C) 2004 Elsevier B.V. All rights reserved.
机译:含手性硼原子的胺-氰基甲氧基羰基硼烷(A.BH(CN)COOMe)的第一个代表是由相应的胺-溴氰基甲氧基羰基硼烷与[BU4N] CN的配合物或由Me3N.BH(CN)COOMe和胺合成的在碱基交换反应中甲酯的酸水解产生了游离酸(A.BH(CN)COOH),它与α-氰基羧酸是等电子的。确定了它们的pK(a)值和在酸性介质中的水解半衰期(即质子还原速率)。类似于α氰基羧酸,连接至硼的氰基(在COOH基的α位)将羧基硼烷的酸强度提高了2.0-2.5个数量级。独立于胺的类型,胺-氰基羧基hor烷(6.34-5.82)的pK(a)值随着胺的pK(b)值的增加而一致地降低。烷基胺配合物的水解分解速率随胺的pKb值增加而增加,而吡啶碱配合物则相反。当考虑两种类型的胺时,配合物的水解半衰期在0.005至400 h的几个数量级范围内。基于这些观察,胺氮原子的质子化似乎是水解过程中的速率决定步骤。随着甲醇的损失,2-NH2-py.BH(CN)COOMe转化为五元内酰胺衍生物。 X射线衍射表明,吡啶环与五元内酰胺环共面。在晶体中,两个分子通过在N(2)-H和羰基氧(01)之间的强分子间H键在头到尾的排列方式连接,给体和受体的距离为2.867(3)A。三个新的氰基甲氧基羰基硼酸酯具有还合成了K [BHn(CN)(3-n)COOMe](n = 1,2)和K [B(OH)(CN)(2-)COOMe]的组成并检查了它们的性能。 (C)2004 Elsevier B.V.保留所有权利。

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