Pincer organometallic complexes in heterogeneous catalysis for organic synthesis and CO2 conversion

• Grant number: 22/11173-2
• Support Opportunities: Scholarships in Brazil - Doctorate
• Start date: December 01, 2022
• Status: Discontinued
• Field of knowledge: Physical Sciences and Mathematics - Chemistry - Inorganic Chemistry
• Principal Investigator: Daniela Zanchet
• Grantee: Davi dos Santos Leite
• Host Institution: Instituto de Química (IQ). Universidade Estadual de Campinas (UNICAMP). Campinas , SP, Brazil
• Company: Universidade de São Paulo (USP). Escola Politécnica (EP)
• Associated research grant: 20/15230-5 - Research Centre for Greenhouse Gas Innovation - RCG2I, AP.PCPE
• Associated scholarship(s): 24/18485-5 - Integrating olefin hydroformylation and alternative syngas sources via dual catalysis, BE.EP.DR

Abstract

The use of accessible synthesis and tunable catalysts is of great interest in both homogeneous and heterogeneous catalysis. In transition metal catalysis, immobilized metal complexes and low-coordinate metal-supported catalysts lie in the interface of these extremes and have in common the ruling effect of metal-support interactions. While these interactions are highly valued in the metal-supported variant, they have only been superficially studied for immobilized metal complexes, especially for supports different from silica and alumina. In this context, this project aims to explore the use of homogeneous pincer transition-metal Pd-organometallic complexes as precursors for both aforementioned catalyst variants, evaluating the effectiveness of the immobilization technique employed, either attaching the support surface to the ligand or directly to the metal center via surface organometallic chemistry. Special attention will be drawn to the different metal-support interactions acting on the catalyst formulations. Additionally, the catalysts synthesized will be applied to the strategic reactions of CO2 conversion and carbon-carbon bond forming cross-coupling reactions, ubiquitous in modern organic chemistry, in both batch and continuous settings.

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

STRAPASSON, GUILHERME B.; BAFERO, GABRIEL B.; LEITE, DAVI S.; SANTOS, DYOVANI B. L.; ALBUQUERQUE, ANGELA; BARCELOS, INGRID D.; ROSSI, LIANE M.; RODELLA, CRISTIANE B.; ZANCHET, DANIELA. Acidity drives selectivity: Tuning reaction pathways of (Pt,Fe)-supported catalysts under hydrodeoxygenation conditions. APPLIED CATALYSIS B-ENVIRONMENTAL, v. 373, p. 16-pg., 2025-09-15. (21/13899-8, 22/11173-2, 20/15230-5, 18/01258-5, 20/12986-1)