Poly(para-arylene)s via [2+2+2]
Author:
Affiliation:
1. Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States
Publisher
American Chemical Society (ACS)
Subject
Materials Chemistry,Inorganic Chemistry,Polymers and Plastics,Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/mz300352m
Reference24 articles.
1. Dehydro coupling of aromatic nuclei by catalyst-oxidant systems: poly(p-phenylene)
2. Synthesis of polyphenylene from a cis-dihydrocatechol biologically produced monomer
3. A Novel Type of Polycondensation Utilizing Transition Metal-Catalyzed C–C Coupling. I. Preparation of Thermostable Polyphenylene Type Polymers
4. Soluble poly(para-phenylene)s. 1. Extension of the Yamamoto synthesis to dibromobenzenes substituted with flexible side chains
5. Blue electroluminescence with ladder-type poly(para-phenylene) and para-hexaphenyl
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1. Preparation of Structurally and Electronically Diverse N → B-Ladder Boranes by [2 + 2 + 2] Cycloaddition;The Journal of Organic Chemistry;2021-10-06
2. Controlled synthesis of unsubstituted high molecular weight poly(para-phenylene) via Suzuki polycondensation-thermal aromatization methodology;Polymer Chemistry;2020
3. Synthesis and molecular crystal of 3-Chloro-2-(1-chloro-1-methyl-ethyl)-2,3-dihydro-1H-naphtho[2,1-b]oxepin-4-one;Journal of Molecular Structure;2018-03
4. Dimensional Evolution of Polyphenylenes: Expanding in All Directions;Chemical Reviews;2015-12-10
5. New Synthetic Approach for Optically Active Polymer Bearing Chiral Cyclic Architecture: Combination of Asymmetric Allylic Amidation and Ring-Closing Metathesis Reaction;Macromolecules;2015-11-16
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