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Updated: Feb 11, 2026

Chemical Dimerization-Induced Protein Condensates on Telomeres
Published on: April 12, 2021
Dimerization of boryl- and amino-substituted acetylenes by B2C2 four-membered ring formation
Ryo Kitamura1, Katsunori Suzuki, Makoto Yamashita
1Department of Applied Chemistry, Graduate School of Science and Engineering, Chuo University, 1-13-27 Kasuga, Bunkyo-ku, Tokyo, 112-8551, Japan.
Abstract:
Boryl- and amino-substituted acetylenes bearing diphenylboryl or 9-borabicyclononyl groups were synthesized. X-ray diffraction analyses revealed the dimerized structures of these acetylenes via the formation of B2C2 four-membered rings. Spectroscopic studies and DFT calculations indicated that these dimers can dissociate to afford monomeric acetylenes, and that the equilibrium constant for the dissociation depends on the structure of the boryl substituents.
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