| Literature DB >> 31859500 |
Javier Urieta-Mora1,2, Marcel Krug3, Wiebke Alex3, Josefina Perles4, Israel Fernández1, Agustín Molina-Ontoria2, Dirk M Guldi3, Nazario Martín1,2.
Abstract
Two novel homo and hetero three-dimensional nanographenes, NG1 and NG2, featuring a cyclooctatetraene core are designed, synthesized, and characterized. A concise and efficient bottom-up methodology was employed during which 24 new carbon-carbon bonds were formed. By means of a Scholl reaction nanographenes with 53 fused rings are realized, which exhibited good solubility in common organic solvents. The resulting saddle-like structures of NG1 and NG2 are electron-rich and show good chemical and electrochemical stability. Their molecular structures are fully elucidated by single-crystal X-ray crystallography. From their crystal structure analysis is concluded that both nanographenes are chiral and crystallize as a racemic mixture. Our work was rounded-off by excited state investigations such as electron and energy transfer with electron-acceptors and -donors.Entities:
Year: 2020 PMID: 31859500 DOI: 10.1021/jacs.9b10203
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419