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膦双官能化双(脒基)-重质四价元素化合物的合成及其一些配位化学:一类此前未知的PEP四价元素化合物(E = Ge和Sn)。

Synthesis and Some Coordination Chemistry of Phosphane-Difunctionalized Bis(amidinato)-Heavier Tetrylenes: A Previously Unknown Class of PEP Tetrylenes (E = Ge and Sn).

作者信息

Cabeza Javier A, García Felipe, García-Álvarez Pablo, García-Soriano Rubén, Pérez-Carreño Enrique

机构信息

Departamento de Química Orgánica e Inorgánica, Centro de Innovación en Química Avanzada ORFEO-CINQA, Universidad de Oviedo, E-33071 Oviedo, Spain.

School of Chemistry, Monash University, Clayton, Victoria 3800, Australia.

出版信息

Inorg Chem. 2023 Sep 25;62(38):15502-15509. doi: 10.1021/acs.inorgchem.3c01953. Epub 2023 Sep 11.

Abstract

The bis(amidinato)-heavier tetrylenes E(bzamP) (E = Ge () and Sn (); bzamP = -isopropyl-'-(diphenylphosphanylethyl)benzamidinate), which are equipped with one heavier tetrylene (germylene or stannylene) and two phosphane fragments (one on each amidinate moiety) as coordinable groups, have been synthesized from the benzamidinum salt [HbzamP]Cl and GeCl(dioxane) or SnCl in 2:1 mol ratio. A preliminary inspection of their coordination chemistry has shown that their amidinate group can also be involved in the bonding with the metal atoms as tridentate ENP and tetradentate PENP' coordination modes have been observed for the ECl(bzamP) ligand of [Ir{κ,,-ECl(bzamP)}(cod)] (E = Ge () and Sn (); cod = η-1,5-cyclooctadiene) and the E(bzamP) ligand of [Ni{κ,,,'-E(bzamP)}] (E = Ge () and Sn ()), which are products of reactions of and with [IrCl(cod)] (1:0.5 mol ratio) and [Ni(cod)] (1:1 mol ratio), respectively. These products contain a 5-membered NCNEM ring that results from the insertion of the metal M atom into an E-N bond of and . Additionally, while iridium(I) complexes and are chloridotetryl derivatives (insertion of the tetrylene E atom into the Ir-Cl bond has also occurred) that have an uncoordinated phosphane group, nickel(0) complexes and contain a tetrylene fragment that, maintaining the lone pair, behaves as a σ-acceptor (-type) ligand.

摘要

双(脒基)-较重的亚四价元素化合物E(bzamP)(E = Ge()和Sn();bzamP = -异丙基-'-(二苯基膦基乙基)苯脒基),其配备有一个较重的亚四价元素(亚锗烯或亚锡烯)和两个膦片段(每个脒基部分一个)作为可配位基团,已由苯脒盐[HbzamP]Cl与GeCl(二氧六环)或SnCl以2:1的摩尔比合成。对其配位化学的初步研究表明,它们的脒基也可参与与金属原子的键合,因为对于[Ir{κ,,-ECl(bzamP)}(cod)](E = Ge()和Sn();cod = η-1,5-环辛二烯)的ECl(bzamP)配体和[Ni{κ,,,'-E(bzamP)}](E = Ge()和Sn())的E(bzamP)配体,已观察到三齿ENP和四齿PENP'配位模式,它们分别是 和 与[IrCl(cod)](1:0.5摩尔比)和[Ni(cod)](1:1摩尔比)反应的产物。这些产物包含一个五元NCNEM环,这是由于金属M原子插入 和 的E-N键中形成的。此外,虽然铱(I)配合物 和 是氯代亚四价元素衍生物(亚四价元素E原子也插入到Ir-Cl键中),具有一个未配位的膦基团,但镍(0)配合物 和 包含一个亚四价元素片段,该片段保持孤对电子,表现为σ-受体(-型)配体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138d/10523440/552aff8f9171/ic3c01953_0001.jpg

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