Formation of Titanosilicate N,N‐dialkyl Carbamates by CO2 Insertion into the [(tBuO)3SiO]3TiNR2 Scaffold

Author:

Pérez‐Pérez Jovana12,Gallardo‐Garibay Alfonso12,Martínez‐Otero Diego12,Hernández‐Balderas Uvaldo12,Jancik Vojtech12ORCID

Affiliation:

1. Universidad Nacional Autónoma de México Instituto de Química Ciudad Universitaria, Ciudad de México 04510 México

2. Centro Conjunto de Investigación en Química Sustentable UAEM-UNAM Carr. Toluca-Atlacomulco km 14.5 50200 Toluca, Estado de México México

Abstract

AbstractMolecular titanosilicates {(tBuO3)3SiO}2Ti(NR2)2 (1, R=Et; 2, R=Me) and {(tBuO3)3SiO}3TiNR2 (TSA1, R=Et; 3, R=Me) were obtained from the reaction between silanol (tBuO3)3SiOH (S1) and titanium amides Ti(NR2)4 (R=Et, R=Me). Additionally, the reaction of 3 and TSA1 with CO2 led to the exclusive formation of carbamates {(tBuO)3SiO}3Ti(O2CNR2) (4, R=Et; 5, R=Me). The molecular structure of 5 confirmed the proposed connectivity and presence of SiO4 and Ti(O2CNR2) units. In compound 4, titanium is coordinated to five oxygen atoms belonging to one bidentate carbamate group and three silicate ligands in a distorted square‐base pyramidal geometry. Also, we have performed DFT calculations and QTAIM analysis to study the distribution of the electron density in the carbamate {(tBuO)3SiO}3Ti(O2CNEt2) (4) and salt {(tBuO)3SiO}3TiO(H2NMe2) 6 which was obtained by the hydrolysis of compound 5.

Publisher

Wiley

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