72 / 2023-09-06 02:59:37
Phosphacyclopentadienide anions – building blocks for organophosphorus chemistry
phospholes,phosphorus,Phosphacyclopentadienide,phosphaferrocenes,asymmetric catalysis,elemental phosphorus
Abstract Accepted
Almaz Zagidullin / Arbuzov Institute of Organic and Physical Chemistry; FRC Kazan Scientific Center of RAS
Phosphacyclopentadienide (phospholide) anions and their derivatives are very attractive as building blocks for the construction of versatile organophosphorus molecular materials with useful and interesting catalytic, optical, luminescent, and magnetic properties.[1] Therefore, development of convenient methods for the straightforward synthesis of these phosphorus heterocycles and their derivatives through functionalization of elemental phosphorus P4 (bypassing toxic chlorine Cl2) has a significant interest.[2] This lecture features recent advances on the synthesis of various phosphacyclopentadienide anions and their chemical behavior toward organic or organoelement substrates, and transition metal complexes. A rational and highly efficient method to access 1-mono-,[3] 1,2-di-[4] and 1,2,3-triphospholide[5] anions in individual forms directly from white phosphorus P4, alkali metals and small molecules (alkynes and cyclopropenylium halides) have been developed. Interaction with various chiral and non-chiral alkyl halides has resulted in the formation of novel P-heterocycles, namely 1-mono-, 1,2-di- and 1,2,3-triphospholes. Reaction with iron(II) complexes was used as a convenient way for an efficient synthesis of a number of new phosphaferrocenes.[6] First results on the application in materials science and homogeneous catalysis of phospholide derivatives (phospholes and their [4+2] cycloadducts) were also reported.[7] This work was supported by the Russian Science Foundation (project no. 21-73-10204).

 
Important Date
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    Nov 12

    2023

    to

    Nov 16

    2023

  • Oct 24 2023

    Draft paper submission deadline

  • Nov 16 2023

    Registration deadline

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Ningbo University
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