首页> 外文期刊>European journal of inorganic chemistry >Reactivity of the pyrazolatopalladium(II) complexes [Pd(dmpz)(2)(Hdmpz)(2)] and [Pd-2(mu-dmpz)(2)(dmpz)(2)(Hdmpz)(2)] towards carboxylic acids: Hydrogen bonds as the driving force that determines the nature of the final products
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Reactivity of the pyrazolatopalladium(II) complexes [Pd(dmpz)(2)(Hdmpz)(2)] and [Pd-2(mu-dmpz)(2)(dmpz)(2)(Hdmpz)(2)] towards carboxylic acids: Hydrogen bonds as the driving force that determines the nature of the final products

机译:吡唑并铝(II)配合物[Pd(dmpz)(2)(Hdmpz)(2)]和[Pd-2(mu-dmpz)(2)(dmpz)(2)(Hdmpz)(2)]的反应性羧酸:氢键作为决定最终产品性质的驱动力

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The compound [Pd(Hdmpz)(4)](O2CCH2NHCOCH3)(2) (1; (Hdmpz = 3,5-dimethylpyrazole) has been obtained by treatment of [Pd(dmpz)(2)(Hdmpz)(2)] (A) with two equivalents of N-acetylglycine (HO2CCH2NHCOCH3). The X-ray study on a crystal of 1 revealed that the N-acetylglycinate anion links to the cationic complex [Pd(HdmpZ)(4)](2+) through the carboxylate group by charge assisted N-H(+)...O(-) hydrogen bonds. Additionally, the remaining N-H and C=O groups allow the N-acetylglycinate anions to self-assemble through N-(HO)-O-... hydrogen bonds to generate infinite chains. The compounds [Pd-2(mu-dmpz)(2)(O2CCH2NHCOCH3-kO)(2)(Hdmpz)(2)] (2) and [Pd-2(mu-dmpz)(2)(O2CC6H4-R-kO)(2)(Hdmpz)(2)] [R = m-NO2 (3a), p-N(CH3)(2) (3b), p-NH2 (3c), p-OCH3 (3d), p-OH (3e)] have been obtained by treatment of [Pd-2(mu-dmpz)(2)(dmpz)(2)-(Hdmpz)(2)] (B) with two equivalents of the monocarboxylic acids N-acetylglycine (HO2CCH2NHCOCH3) and the benzoic derivatives HO2CC6H4R [R = m-NO2, p-N(CH3)(2), p-NH2, p-OCH3, p-OH] respectively. The X-ray study on complexes 3d and 3e shows that in these complexes the carboxylate anion bonded to one Pd atom and the terminal Hdmpz group bonded to the other one have the right arrangement to establish an N-(HO)-O-... hydrogen bond. The (HO)-O-... and (NO)-O-... distances are in the range of those corresponding to charge-assisted N-H(+)...O(-) interactions. In complexes 3a-3e, the H atoms of the terminal Hdmpz groups can be replaced by Ag+ to give the mixed-metal complexes [Pd2Ag2(mu-dmpz)(4)(mu-O2CC6H4-R-kO)(2)(Hdmpz)(2)] [R = m-NO2 (4a), p-N(CH3)(2) (4b), p-NH2 (4c), p-OCH3 (4d), p-OH (4e)]. Compounds 4a-4e, which exhibit a transoid conformation of the carboxylate groups with respect to the (PdPd)-Pd-... line, isomerise to the cisoid species (4a'-4e'). The X-ray structure of the DMSO adduct of 4d' is also reported. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006).
机译:通过处理[Pd(dmpz)(2)(Hdmpz)(2)]获得了化合物[Pd(Hdmpz)(4)](O2CCH2NHCOCH3)(2)(1;(Hdmpz = 3,5-二甲基吡唑) (A)与两个当量的N-乙酰基甘氨酸(HO2CCH2NHCOCH3)。对1晶体的X射线研究表明,N-乙酰基甘氨酸阴离子通过阳离子与阳离子配合物[Pd(HdmpZ)(4)](2+)连接通过电荷辅助的NH(+)... O(-)氢键形成羧酸根基团;此外,剩余的NH和C = O基团使N-乙酰基甘氨酸根阴离子通过N-(HO)-O-自组装。 ..氢键生成无限链。化合物[Pd-2(mu-dmpz)(2)(O2CCH2NHCOCH3-kO)(2)(Hdmpz)(2)](2)和[Pd-2(mu-dmpz )(2)(O2CC6H4-R-kO)(2)(Hdmpz)(2)] [R = m-NO2(3a),pN(CH3)(2)(3b),p-NH2(3c),p -OCH3(3d),p-OH(3e)]是通过用两种方法处理[Pd-2(mu-dmpz)(2)(dmpz)(2)-(Hdmpz)(2)](B)而获得的一元羧酸N-乙酰基甘氨酸(HO2CCH2NHCOCH3)和苯甲酸酯衍生物HO2CC6H4R的当量[R = m-NO2,pN(CH3)(2),p-NH2,p-OCH3,p-OH ] 分别。对配合物3d和3e进行的X射线研究表明,在这些配合物中,键合到一个Pd原子上的羧酸根阴离子和键合到另一个Pd原子上的末端Hdmpz基团具有正确的排列方式以建立N-(HO)-O-。 。 氢键。 (HO)-O -...和(NO)-O -...的距离在与电荷辅助的N-H(+)... O(-)相互作用相对应的范围内。在配合物3a-3e中,末端Hdmpz基团的H原子可以被Ag +取代,从而得到混合金属配合物[Pd2Ag2(mu-dmpz)(4)(mu-O2CC6H4-R-kO)(2)(Hdmpz )(2)] [R = m-NO 2(4a),pN(CH 3)(2)(4b),p-NH 2(4c),p-OCH 3(4d),p-OH(4e)]。相对于(PdPd)-Pd -...线表现出羧酸根基团的反式构象的化合物4a-4e异构化为顺式物质(4a′-4e′)。还报道了4d'的DMSO加合物的X射线结构。 ((c)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,德国,2006年)。

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