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含镍和钯的三氨基硼烷桥联二膦配合物:配位化学、结构及配体中心反应活性

Triaminoborane-bridged diphosphine complexes with Ni and Pd: coordination chemistry, structures, and ligand-centered reactivity.

作者信息

Lee Kyounghoon, Donahue Courtney M, Daly Scott R

机构信息

The University of Iowa, Department of Chemistry, E331 Chemistry Building, Iowa City, IA 52242-1294, USA.

出版信息

Dalton Trans. 2017 Jul 25;46(29):9394-9406. doi: 10.1039/c7dt02144e.

Abstract

The synthesis, coordination chemistry, and reactivity of two diphosphines containing the cyclic triaminoborane 1,8,10,9-triazaboradecalin (TBD) are described. To evaluate the ligand-centered reactivity of TBDPhos and TBDPhos, the complexes (TBDPhos)MCl and (TBDPhos)MCl, where M = Ni and Pd, were prepared and characterized by elemental analysis, multinuclear NMR spectroscopy (H, C, P, and B), and single-crystal X-ray diffraction (XRD). Despite very low boron Lewis acidity in the TBD backbone, (TBDPhos)NiCl (1) and (TBDPhos)PdCl (3) react with HO, alcohols, and hydrated fluoride reagents in the presence of NEt to yield trans H-O or H-F addition across the bridgehead N-B bond. In contrast, TBDPhos shows no appreciable reactivity when bound to NiCl (2) and PdCl (4), which is attributed to the sterically-bulky isopropyl substituents blocking substrate access to boron in the TBD backbone. The new complexes {(TBDPhos-HO)Ni}Cl (5), {(TBDPhos-HO)Pd}Cl (6), (TBDPhos-MeOH)NiCl (7), (TBDPhos-MeOH)PdCl (8), (TBDPhos-CHOH)PdCl (9), and {(TBDPhos-HF)Ni}Cl (10) were isolated, and all but 6 were structurally characterized by single-crystal XRD. Multinuclear NMR studies revealed that isolated, crystallographically-authenticated samples of 5-9 lose ligand-bound water or alcohol with reappearance of starting materials 1 and 3 when dissolved in NMR solvents. Addition of NEt attenuated the water and alcohol loss from 5-9 to allow H, C, P, and B NMR data to be collected for all the compounds, confirming the determined structures. Additional reactivity experiments with NaOMe and fluoride reagents suggested that participation of the bridgehead nitrogen in the TBD backbone is important for promoting reactivity at boron when TBDPhos is bound to Ni and Pd. The term "cooperative ligand-centered reactivity" (CLR) is proposed to define chemical reactions that appear to require participation of more than one atom on the ligand, such as those reported here.

摘要

本文描述了两种含有环状三氨基硼烷1,8,10,9 - 三氮杂硼十氢化萘(TBD)的二膦配体的合成、配位化学及反应活性。为评估TBDPhos和TBDPhos以配体为中心的反应活性,制备了配合物(TBDPhos)MCl和(TBDPhos)MCl(其中M = Ni和Pd),并通过元素分析、多核核磁共振光谱(H、C、P和B)以及单晶X射线衍射(XRD)对其进行了表征。尽管TBD主链中的硼路易斯酸性很低,但(TBDPhos)NiCl(1)和(TBDPhos)PdCl(3)在NEt存在下与HO、醇类和水合氟试剂反应,可在桥头N - B键上实现反式H - O或H - F加成。相比之下,TBDPhos与NiCl(2)和PdCl(4)配位时没有明显的反应活性,这归因于空间位阻较大的异丙基取代基阻碍了底物接近TBD主链中的硼。分离得到了新的配合物{[(TBDPhos - HO)Ni](μ - OH)}Cl(5)、{[(TBDPhos - HO)Pd](μ - OH)}Cl(6)、(TBDPhos - MeOH)NiCl(7)、(TBDPhos - MeOH)PdCl(8)、(TBDPhos - CHOH)PdCl(9)和{[(TBDPhos - HF)Ni](μ - OH)}Cl(10),除6外的所有配合物均通过单晶XRD进行了结构表征。多核核磁共振研究表明,分离得到的经晶体学验证的5 - 9样品在溶解于核磁共振溶剂时会失去配体结合的水或醇,重新出现起始原料1和3。加入NEt可减少5 - 9中水分和醇的损失,从而能够收集所有化合物的H、C、P和B核磁共振数据,证实了所确定的结构。用NaOMe和氟试剂进行的其他反应实验表明,当TBDPhos与Ni和Pd配位时,TBD主链中桥头氮的参与对于促进硼的反应活性很重要。本文提出了“协同配体中心反应活性”(CLR)这一术语来定义似乎需要配体上多个原子参与的化学反应,比如本文所报道的这些反应。

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