Macromolecular helicity control of poly(phenyl isocyanate)s with a single stimuli-responsive chiral switch-Reference-Cited by-同舟云学术

Macromolecular helicity control of poly(phenyl isocyanate)s with a single stimuli-responsive chiral switch

Published:2019 Issue:55 Volume:55 Page:7906-7909
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Fukuda Mayu¹²³⁴,Rodríguez Rafael⁵²³⁴,Fernández Zulema⁶⁷⁸⁹,Nishimura Tatsuya¹²³⁴,Hirose Daisuke¹²³⁴⁵,Watanabe Go¹⁰¹¹¹²⁴^ORCID,Quiñoá Emilio⁶⁷⁸⁹,Freire Félix⁶⁷⁸⁹^ORCID,Maeda Katsuhiro¹²³⁴⁵^ORCID

Affiliation:

1. Graduate School of Natural Science and Technology

2. Kanazawa University

3. Kanazawa 920-1192

4. Japan

5. WPI Nano Life Science Institute (WPI-NanoLSI)

6. Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS) and Departamento de Química Orgánica

7. Universidade de Santiago de Compostela

8. Santiago de Compostela

9. Spain

10. School of Science

11. Kitasato University

12. Sagamihara

Abstract

The macromolecular helicity of poly(phenyl isocyanate)s can be tuned by a conformational switch of the chiral initiator through a domino effect.

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science and Technology

Xunta de Galicia

European Regional Development Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CC/C9CC03555A

Reference48 articles.

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4. Three-State Switchable Chiral Stationary Phase Based on Helicity Control of an Optically Active Poly(phenylacetylene) Derivative by Using Metal Cations in the Solid State

5. High-Molecular-Weight Polyquinoxaline-Based Helically Chiral Phosphine (PQXphos) as Chirality-Switchable, Reusable, and Highly Enantioselective Monodentate Ligand in Catalytic Asymmetric Hydrosilylation of Styrenes

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