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Aluminum-Boron Bond Formation by Boron Ester Oxidative Addition at an Alumanyl Anion.


ABSTRACT: The potassium diamidoalumanyl, [K{Al(SiNDipp)}]2 (SiNDipp = {CH2SiMe2NDipp}2), reacts with the terminal B-O bonds of pinacolato boron esters, ROBpin (R = Me, i-Pr), and B(OMe)3 to provide potsassium (alkoxy)borylaluminate derivatives, [K{Al(SiNDipp)(OR)(Bpin)}]n (R = Me, n = 2; R = i-Pr, n = ∞) and [K{Al(SiNDipp)(OMe)(B(OMe)2)}], comprising Al-B σ bonds. An initial assay of the reactivity of these species with the heteroallene molecules, N,N'-diisopropylcarbodiimide and CO2, highlights the kinetic inaccessibility of their Al-B bonds; only decomposition at high temperature is observed with the carbodiimide, whereas CO2 preferentially inserts into the Al-O bond of [K{Al(SiNDipp)(OMe)(Bpin)}]2 to provide a dimeric methyl carbonate species. Treatment of the acyclic dimethoxyboryl species, however, successfully liberates a terminal alumaboronic ester featuring trigonal N2Al-BO2 coordination environments at both boron and aluminum.

SUBMITTER: Liu HY 

PROVIDER: S-EPMC10521018 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature

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Aluminum-Boron Bond Formation by Boron Ester Oxidative Addition at an Alumanyl Anion.

Liu Han-Ying HY   Mahon Mary F MF   Hill Michael S MS  

Inorganic chemistry 20230906 37


The potassium diamidoalumanyl, [K{Al(SiN<sup>Dipp</sup>)}]<sub>2</sub> (SiN<sup>Dipp</sup> = {CH<sub>2</sub>SiMe<sub>2</sub>NDipp}<sub>2</sub>), reacts with the terminal B-O bonds of pinacolato boron esters, ROBpin (R = Me, <i>i</i>-Pr), and B(OMe)<sub>3</sub> to provide potsassium (alkoxy)borylaluminate derivatives, [K{Al(SiN<sup>Dipp</sup>)(OR)(Bpin)}]<i><sub>n</sub></i> (R = Me, <i>n</i> = 2; R = <i>i</i>-Pr, <i>n</i> = ∞) and [K{Al(SiN<sup>Dipp</sup>)(OMe)(B(OMe)<sub>2</sub>)}]<sub>∞</sub>,  ...[more]

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