This Forum review describes the most recent achievements in the novel prospective field of highly reactive main-group organometallics, namely, geminal dianionic derivatives of the heavy group 14 elements (Si, Ge, Sn). A brief historical introduction to the topic is followed by discussion of the current state of affairs in the field of stable derivatives and prospects for future efforts, highlighting our own synthetic approach and recent results. The most important experimental contributions, including synthesis of 1,1-dilithiosilane, -germane, and -stannane derivatives; dilithio(halo)silanes (lithiosilylenoids); metallole 1,1-dianions; and heavy analogues of the cyclobutadiene dianion derivatives, are presented, along with a discussion of the synthetic applications of the above-mentioned organometallic compounds.
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http://dx.doi.org/10.1021/ic2006106 | DOI Listing |
Chemistry
October 2023
Laboratoire Hétérochimie Fondamentale et Appliquée, LHFA UMR CNRS 5069, Université Paul Sabatier, CNRS, 118 Route de Narbonne, 31062, Toulouse, France.
Numerous synthetic models of the FeMo-co cluster of nitrogenases have been proposed to find the simplest structure with relevant reactivity. Indeed, such structures are able to perform multi-electrons reduction processes, such as the conversion of N to ammonia, and of CO into methane and alkenes. The most challenging parameter to imitate is indeed the central carbide ligand, which is believed to maintain the integrity of iron sulfide assembly during the course of catalytic cycles.
View Article and Find Full Text PDFBeilstein J Org Chem
August 2020
Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
Dilithio sulfonyl methandiides are a synthetically and structurally highly interesting group of functionalized geminal dianions. Although very desirable, knowledge of the structure of dilithio methandiides in solution was lacking up to now. Herein, we describe the isolation and determination of the structure of tetrameric dilithio (trimethylsilyl)(phenylsulfonyl) methandiide in solution and in the crystal.
View Article and Find Full Text PDFChem Rev
July 2019
UPS, CNRS, LHFA UMR 5069 , Université de Toulouse, 118 Route de Narbonne , 31062 Toulouse , France.
This review is dedicated to the chemistry of stable and isolable species that bear two lone pairs at the same C center, i.e., geminal dianions, stabilized by main group elements.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2017
Laboratoire Hétérochimie Fondamentale et Appliquée, Université Paul Sabatier/CNRS UMR 5069, 118 Route de Narbonne, 31062, Toulouse Cedex, France.
The first Au carbene complex was prepared by reacting a geminal dianion with a (P,C) cyclometalated Au precursor. Its structure and bonding situation have been thoroughly investigated by experimental and computational means. The presence of a high-energy highest occupied molecular orbital (HOMO) centered at the carbene center suggests nucleophilic character for the Au carbene complex.
View Article and Find Full Text PDFJ Am Chem Soc
January 2015
Division of Chemistry and Biotechnology, Graduate School of Natural Science and Technology and ‡Research Center of New Functional Materials for Energy Production, Storage, and Transport, Okayama University, 3-1-1 Tsushimanaka, Kita-ku, Okayama 700-8530, Japan.
Treatment of gem-di(iodozincio)methane with pyridine or diamine derivatives resulted in the isolation of a storable gem-di(iodozincio)methane species. Use of the sterically bulky bipyridine ligand gave a gem-di(iodozincio)methane complex, which allowed the first X-ray structural analysis of such species. This work represents a rare example of the isolation of an organometallic reactive species in Schlenk equilibrium and thus provides new insight into the design of efficient and storable organometallic reagents.
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