...
首页> 外文期刊>Inorganica Chimica Acta >DO PARAMAGNETIC PLATINUM METAL HYDRIDES REALLY EXIST - A REINVESTIGATION OF THE SYNTHESIS AND MAGNETOCHEMICAL PROPERTIES OF IR(H)(X)(CL)(2)(P-I-PR-3)(2) (1) - SYNTHESES AND CRYSTAL STRUCTURE DETERMINATIONS OF TRANS-IR(H)(CL)(2)(CO)(P-I-PR-3)(2) (2),
【24h】

DO PARAMAGNETIC PLATINUM METAL HYDRIDES REALLY EXIST - A REINVESTIGATION OF THE SYNTHESIS AND MAGNETOCHEMICAL PROPERTIES OF IR(H)(X)(CL)(2)(P-I-PR-3)(2) (1) - SYNTHESES AND CRYSTAL STRUCTURE DETERMINATIONS OF TRANS-IR(H)(CL)(2)(CO)(P-I-PR-3)(2) (2),

机译:是否确实存在过顺铂金属氢化物-IR(H)(X)(CL)(2)(PI-PR-3)(2)(1)的合成和磁化学性质的再研究-的合成和晶体结构的测定TRANS-IR(H)(CL)(2)(CO)(PI-PR-3)(2)(2),

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

As further studies of our samples of Ir(H)(x)(Cl)(2)(P-i-Pr-3)(2) (1) led us to suspect that their paramagnetism was due to cooperative surface phenomena we decided a through reinvestigation of the system 1. The reaction of ethanolic solution of H-2[IrCl6] with P-i-Pr-3, in the presence of concentrated HCl, gave compound 1 in 70% yield. The magnetic moment of this sample does not exceed 0.5 BM. Washing the sample with water or with organic solvents and crushing it with a platinum spatula gave an increase in mu(eff). H-1 spin-lattice relaxation (T-1) measurement on solid samples of 1 at different mu(eff) values (0.5, 1.5 BM) suggest that the paramagnetism is due to cooperative surface phenomena and the bulk of 1 is diamagnetic. As found in the complex prepared starting from (NH4)(2)[IrCl6], the above sample shows two weak bands at 2116 and 2002 cm(-1). These, however, are not due to v(lr-H) but to the presence of small amounts of two carbonyl complexes. By bubbling CO gas into an ethanolic solution of 1, the trans-Ir(H) (Cl)(2)(CO) (P-i-Pr-3)(2) (2) compound is obtained. This carbonyl complex shows an extremely strong band at 2002 cm(-1). Trans-2, both in solution and in the solid state, isomerizes into cis-Ir(H) (Cl)(2)(CO) (P-i-Pr-3)(2) (4). By reacting an ethanolic solution of H-2[IrCl6] with P-i-Pr-3, without addition of HCl, a mixture of 1 and another complex, trans-Ir(Cl) (CO) (P-i-Pr-3)(2) (5), is obtained, characterized by a strong band at 1930 cm(-1). Subsequent refluxing of the mother liquor of the above synthesis gave pure 5. This new complex is responsible for the very strong band at 1930 cm(-1). Thus, the v(Ir-H) of complex 1 does not occur in the usual region, and may be masked by the H2O absorption at ca. 1700-1600 cm(-1). Crystallographic data: for trans-2 (at 298 K), a=15.515(6), b=8.633(4), c=19.521(9) Angstrom, beta=104.34(3)degrees in space group Ia (Z=4). For cis-4 (at 298 K), a=16.488(1), b=27.118(2), c=11.384(1) A in space group Pbca (Z=8). For trans-5 (at 298 K), a=8.152(3), b=8.918(3), c=16.639(6) Angstrom, beta=93.50(3)degrees in space group P2(1)/c (Z=2). [References: 28]
机译:随着对Ir(H)(x)(Cl)(2)(Pi-Pr-3)(2)(1)样品的进一步研究导致我们怀疑它们的顺磁性是由于合作表面现象引起的,我们决定通过系统的再研究1.在浓盐酸存在下,H-2 [IrCl6]的乙醇溶液与Pi-Pr-3进行反应,得到化合物1,产率为70%。该样品的磁矩不超过0.5 BM。用水或有机溶剂洗涤样品,并用铂金刮刀压碎,亩数增加。在不同的mu(eff)值(0.5、1.5 BM)下对1的固体样品进行的H-1自旋晶格弛豫(T-1)测量表明,顺磁性是由于表面合作现象引起的,而1的大部分是反磁性的。从(NH4)(2)[IrCl6]开始制备的络合物中发现,上述样品在2116和2002 cm(-1)处显示两个弱带。然而,这些不是由于v(lr-H),而是由于存在少量的两种羰基配合物。通过将CO气体鼓泡到1的乙醇溶液中,获得反式-Ir(H)(Cl)(2)(CO)(P-i-Pr-3)(2)(2)化合物。该羰基配合物在2002 cm(-1)处显示出非常强的谱带。溶液和固态中的Trans-2均异构化为顺式-Ir(H)(Cl)(2)(CO)(P-i-Pr-3)(2)(4)。通过在不添加HCl的情况下使H-2 [IrCl6]的乙醇溶液与Pi-Pr-3反应,将1和另一种复杂的反式Ir(Cl)(CO)(Pi-Pr-3)(2)的混合物)(5),其特征是在1930 cm(-1)处有很强的带。随后上述合成的母液回流,得到纯净的5。这种新的络合物是1930 cm(-1)处非常强的谱带的原因。因此,络合物1的v(Ir-H)不会在通常区域中出现,并且可能会被大约2的H2O吸收所掩盖。 1700-1600厘米(-1)。晶体学数据:对于trans-2(在298 K下),a = 15.515(6),b = 8.633(4),c = 19.521(9)埃,beta = 104.34(3)度在空间群Ia中(Z = 4 )。对于cis-4(在298 K下),空间群Pbca(Z = 8)中的a = 16.488(1),b = 27.118(2),c = 11.384(1)A.对于trans-5(在298 K时),a = 8.152(3),b = 8.918(3),c = 16.639(6)埃,beta = 93.50(3)度在空间群P2(1)/ c(Z = 2)。 [参考:28]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号