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首页> 外文期刊>Chemistry: A European journal >Selective C-C Bond Formation between Alkynes Mediated by the [RuCp(PR_3)]~+ Fragment Leading to Allyl, Butadienyl, and Allenyl Carbene Complexes-An Experimental and Theoretical Study
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Selective C-C Bond Formation between Alkynes Mediated by the [RuCp(PR_3)]~+ Fragment Leading to Allyl, Butadienyl, and Allenyl Carbene Complexes-An Experimental and Theoretical Study

机译:由[RuCp(PR_3)]〜+片段介导的烯丙基之间的选择性C-C键形成,导致烯丙基,丁二烯基和烯丙基碳烯配合物-实验和理论研究

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The reaction of alkynes with [RuCp(PR_3)(CH_3CN)_2]PF_6 (R = Me, Ph, Cy) affords, depending on the structure of the alkynes and the substituent of the phosphine ligand, allyl carbene or butadienyl carbene complexes. These reactions involve the migration of the phosphine ligand or a facile 1,2 hydrogen shift. Both reactions proceed via a metallacyclopentatriene complex. If no #alpha#C-H bonds are accessible, allyl carbenes are formed, while in the presence of #alpha#C-H bonds butadienyl carbenes are typically obtained. With diphenylacetylene, on the other hand, a cyclobutadiene complex is formed. A different reaction pathway is encountered with HC(ident to)CSiMe_3, ethynylferrocene (HC(ident to)CFc), and ethynylruthenocene (HC(icent to)CRc). Whereas the reaction of [RuCp(PR_3)(CH_3CN)_2]PF_6 (R = Ph and Cy) with HC(icent to)CsiMe_3 affords a vinylidene complex, with HC(icent to)CFc and HC(icent to)CRc this reaction does not stop at the vinylidene stage but subsequent cycloaddition yields allenyl carbene complexes. This latter C-C bond formation is effected by strong electronic coupling of the metallocene moiety with the conjugated allenyl carbene unit, which facilitates transient vinylidene formation with subsequent alkyne insertion into the Ru=C bond The vinylidene intermediate appears only in the presence of bulky substituents of the phosphine coligand. For the small R = Me, head-to-tail coupling between two alkyne molecules involving phosphine migration is preferred, giving the more usual allyl carbene complexes. X-ray structures of representative complexes are presented. A reasonable mechanism for the formation of both allyl and allenyl carbenes have been established by means of DFT calculations. During the formation of allyl and allenyl carbenes, metallacyclopentatriene and vinylidene complexes, respectively, are crucial intermediates.
机译:炔烃与[RuCp(PR_3)(CH_3CN)_2] PF_6(R = Me,Ph,Cy)的反应提供,这取决于炔烃的结构和膦配体的取代基,烯丙基卡宾或丁二烯卡宾配合物。这些反应涉及膦配体的迁移或容易的1,2氢转移。两个反应均通过金属环戊三烯配合物进行。如果没有#α#C-H键可及,则形成烯丙基碳烯,而在存在#α#C-H键的情况下,通常获得丁二烯基碳烯。另一方面,与二苯乙炔一起形成环丁二烯配合物。 HC(与CSiMe_3相同),乙炔基二茂铁(HC(与CFc相同))和乙炔基钌茂金属(HC(与CRc相同))会遇到不同的反应途径。而[RuCp(PR_3)(CH_3CN)_2] PF_6(R = Ph和Cy)与HC(至)CsiMe_3的反应可得到亚乙烯基络合物,其中HC(至)CFc和HC(至)CRc在亚乙烯基阶段不停止,但是随后的环加成产生烯丙基卡宾配合物。后者的CC键形成是通过茂金属部分与共轭的烯基碳烯单元的强电子偶联来实现的,这有利于瞬态亚乙烯基的形成,随后炔烃插入Ru = C键中。亚乙烯基中间体仅在存在较大取代基的情况下出现。膦大肠菌素。对于小的R = Me,优选两个涉及膦迁移的炔烃分子之间的头对尾偶联,得到更常见的烯丙基卡宾配合物。介绍了代表性复合物的X射线结构。通过DFT计算已经建立了形成烯丙基和烯丙基碳烯的合理机理。在烯丙基和烯丙基碳烯形成期间,金属环戊三烯和亚乙烯基络合物分别是关键的中间体。

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