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Synthesis and properties of oligo(biradicals) composed of 1,3‐diphosphacyclobutane‐2,4‐diyl units and benzyl‐type linkers

2010/01/01 by Shigekazu Ito, Joji Miura, Noboru Morita +2 · 1 citation
Chemistry · #Synthesis and characterization of novel inorganic/organometallic compounds #Organometallic Complex Synthesis and Catalysis #Ferrocene Chemistry and Applications #Chemistry #Heteroatom #Steric effects #Dimer #Stereochemistry #Medicinal chemistry #Organic chemistry #Ring (chemistry)

paper · doi:10.1002/hc.20625

openalex publication_date 2010/01/01 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/23

Abstract

Abstract We have succeeded in catenating two sterically encumbered 1,3‐di‐ t ‐butyl‐2,4‐bis(2,4,6‐tri‐ t ‐butylphenyl)‐1,3‐diphosphacyclobutane‐2,4‐diyl units with a spacer 1,2‐(CH 2 ) 2 C 6 H 4 to obtain bis(biradicals) as considerably stable compounds. We have discussed physicochemical properties of the dimer, together with DFT calculations of model compounds. Spectroscopic data, redox properties, and X‐ray structures of the oligo(biradicals) derivatives including other spacers like 1,3‐(CH 2 ) 2 C 6 H 4 , 1,4‐(CH 2 ) 2 C 6 H 4 , and 1,3,5‐(CH 2 ) 3 C 6 H 3 , reveal that the P‐heterocyclic biradical moieties interact through nonconjugative pathways. These properties of oligo(biradicals) will facilitate to design novel molecular systems for electronics. © 2010 Wiley Periodicals, Inc. Heteroatom Chem 21:404–411, 2010; View this article online at wileyonlinelibrary.com . DOI 10.1002/hc.20625

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