Journal Article10.1021/CR100133Q
π-Bonding and the Lone Pair Effect in Multiple Bonds Involving Heavier Main Group Elements: Developments in the New Millennium
Roland Fischer,Philip P. Power +1 more
980
TL;DR: The key unifying feature of almost all molecules discussed in this review is that they are generally stabilized by the use of bulky substituents which block associative or various decomposition pathways.
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Abstract: This review is essentially an update of one entitled “πBonding and The Lone Pair Effect in Multiple Bonds Between Heavier Main Group Elements” which was published more than 10 years ago in this journal.1 The coverage of that survey was focused on the synthesis, structure, and bonding of stable compounds2 of heavier main group elements that correspond to the skeletal drawings reproduced in Tables 1 and 2. A row of numbers is listed at the bottom of each column in these tables. This refers to the number of stable complexes from each class that are currently known. The numbers in parentheses refer to the number of stable species that were known at the time of the previous review. Clearly, many of the compound classes listed have undergone considerable expansion although some remain stubbornly rare. The most significant developments for each class will be discussed in detail under the respective sections. As will be seen, there are also a limited number of multiple bonded heavier main group species that do not fit neatly in the classifications in Tables 1 and 2. However, to keep the review to a manageable length, the limits and exclusions, which parallel those used earlier, are summarized as follows: (i) discussion is mainly confined to compounds where experimental data on stable, isolated species have been obtained, (ii) stable compounds having multiple bonding between heavier main group elements and transition metals are not generally discussed, (iii) compounds in which a multiple bonded heavier main group element is incorporated within a ring are generally not covered, and (iv) hypervalent main group compounds that may incorporate faux multiple bonding are generally excluded. Such compounds are distinguished from those in Tables 1 and 2 in that they apparently require the use of more than four valence bonding orbitals at one or more of the bonded atoms. The remainder of this review is organized in a similar manner to that of the previous one wherein the compounds to be discussed are classified according to those summarized in Tables 1 and 2. The key unifying feature of almost all molecules discussed in this review is that they are generally stabilized by the use of bulky substituents which block associative or various decomposition pathways.3 Since the previous review was published in 1999, several review articles that cover parts of the subject matter have appeared.4
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Compounds containing λ3,σ2-SbC bonds: synthesis and structural characterisation of the first stiba-enol, Mes*C(O)SbC(OH)Mes* (Mes* = C6H2But3-2,4,6) and a 2,3-distibabutadiene, {Mes(Me3SiO)CSb}2 (Mes = C6H2Me3-2,4,6)†
TL;DR: In this paper, the reactions of [Li{Sb(SiMe3)2}] with RCOCl, R = C6H2But3-2,4,6 (Mes*) or C6Me3SiO)CSb}2 can be protonated to give the first stiba-enol, Mes*C(O)SbC(OH)Mes*, which has been structurally characterised.
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Thermal Reactions of 5‐Alkylidene‐4,5‐dihydro‐3H‐1,2,4(λ3)‐diazaphospholes (4‐Phosphapyrazolines) – A Route to Various PHeterocycles and to 2‐Phosphabutadienes
TL;DR: The 5-alkylidene-4,5-dihydro-3H-1,2,4(λ3)-diazaphospholes (4-phosphapyrazolines) are thermally much more stable than related compounds without the exocyclic double bond as mentioned in this paper.
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The interaction of phosphavinyl Grignard reagents with group 15 halides: synthesis and structural characterisation of novel heterocyclic and heterocage compounds
TL;DR: In this article, the reactions of a phosphavinyl Grignard reagent, [CyPC(But)MgCl(OEt2)], with a variety of group 15 halide compounds in a number of stoichiometries have been investigated.
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Novel trichlorosilylation and trichlorogermylation of a P-chlorophosphaalkene leading to functionally substituted diphosphenes
TL;DR: The reactions of P-chlorobis(trimethylsilyl)methylenephosphane with hexachlorodisilane or with dichlorogermylene-dioxane afford the new Si-functionalised ditrisyldiphosphene derivative [(Me 3 Si) 2 (Cl 3 Si)-CP] 2 and the related trichloroglomermyl diphosphenes.
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Synthesis of phosphaformamidines and phosphaformamidinates.
TL;DR: A large-scale synthetic route to a variety ofPhosphaformamidines and phospha formamidinates, a type of derivative that was not accessible by the methods previously known for preparingphosphaamids, is reported.
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