Agencia Estatal de Investigación
2023-12-11
The homolytic elimination of two H atoms from two adjacent carbons in benzene results in the aromatic product o-benzyne. In a similar way, the homolytic elimination of two H atoms from the two adjacent carbons in 1,2-C2B10H12 results in the aromatic product o-carboryne. In this work, we provide experimental and computational evidences that despite the similarity of o-carboryne and o-benzyne, the nature of the C-C bond generated between two adjacent carbons that lose H atoms is different. While in o-benzyne the C-C bond behaves as a triple bond, in o-carboryne the C-C bond is a double bond. Therefore, we must stop naming o-carboryne to 1,2-dehydro-o-carborane but to call it o-carborene
Ministerio de Ciencia e Innovación. Grant Numbers: PID2020-113711GB-I00, PID2019-106830GB-I00, PID2022-138861NB-I00, PID2019-106832RB-100, CEX2021-001202-M
Article
Published version
peer-reviewed
English
Benzè; Carborans; Enllaços químics; Benzene; Carboranes; Chemical bonds; Aromaticitat (Química); Aromaticity (Chemistry)
Wiley
info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.202302448
info:eu-repo/semantics/altIdentifier/issn/0947-6539
info:eu-repo/semantics/altIdentifier/eissn/1521-3765
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-113711GB-I00/ES/DISEÑO Y SINTESIS DE FULLERENOS PARA LA CONSTRUCCION DE CELDAS SOLARES HIBRIDAS DE PEROVSKITA Y FULERENOS D ALTO RENDIMIENTO. UN ENFOQUE EXPERIMENTAL Y COMPUTACIONAL SINERGICO/
Reconeixement 4.0 Internacional
http://creativecommons.org/licenses/by/4.0