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Trihalide-included (I-2, Br-2 and IBrCl-) bambus[6]urils in halogenation and iodine-catalysed reactions

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Author(s):
Cicolani, Renato Salviato ; de Oliveira-Filho, Antonio Gustavo Sampaio ; de Lima Batista, Ana Paula ; Demets, Gregoire Jean-Francois
Total Authors: 4
Document type: Journal article
Source: JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY; v. N/A, p. 7-pg., 2023-02-13.
Abstract

We have prepared two new heterotrihalides inside methyl-bambus[6]uril, [Br2Cl](-)@MeBU[6] and [BrICl](-)@MeBU[6], both in solution and in the solid state. These heterotrihalides were used alongside with the first one our group has produced, [I2Cl](-)@MeBU[6], as halogenation agents in classical halogenation and iodine-based catalysts for organic reactions, with comparable yields to those obtained with pure dihalogens. (AU)

FAPESP's process: 17/18238-4 - Catalytic C-H activation reactions: computational study aiming atom efficiency in CO2 fixation
Grantee:Ana Paula de Lima Batista
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 16/12666-1 - Chemical and physical properties of bamabusurils, semi-cucurbiturils and calix4azulenes: three neglected cavitands
Grantee:Grégoire Jean-François Demets
Support Opportunities: Regular Research Grants
FAPESP's process: 17/19595-5 - Properties and applications for the bambus6uril cavitand
Grantee:Renato Salviato Cicolani
Support Opportunities: Scholarships in Brazil - Doctorate
FAPESP's process: 15/11714-0 - Reactivity, transformation, fixation, and spectroscopy of systems involving CO2
Grantee:Antonio Gustavo Sampaio de Oliveira Filho
Support Opportunities: Regular Research Grants