Pristine Poly(para-phenylene): Relating Semiconducting Behavior to Kinetics of Precursor Conversion-Reference-Cited by-同舟云学术

Pristine Poly(para-phenylene): Relating Semiconducting Behavior to Kinetics of Precursor Conversion

Published:2019-05-03 Issue:21 Volume:11 Page:19481-19488
ISSN:1944-8244
Container-title:ACS Applied Materials & Interfaces
language:en
Short-container-title:ACS Appl. Mater. Interfaces

Author:

Strunk Karl-Philipp¹²,Abdulkarim Ali³⁴,Beck Sebastian¹³^ORCID,Marszalek Tomasz⁵,Bernhardt Jakob¹³,Koser Silke⁴,Pisula Wojciech⁵^ORCID,Jänsch Daniel³⁴,Freudenberg Jan³⁴,Pucci Annemarie¹²³^ORCID,Bunz Uwe H. F.³⁴^ORCID,Melzer Christian¹²³,Müllen Klaus³⁵^ORCID

Affiliation:

1. Kirchhoff-Institut für Physik, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 227, 69120 Heidelberg, Germany

2. Centre for Advanced Materials, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 225, 69120 Heidelberg, Germany

3. InnovationLab, Speyerer Straße 4, 69115 Heidelberg, Germany

4. Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany

5. Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany

Funder

German Federal Ministry of Education and Research (BMBF)

Publisher

American Chemical Society (ACS)

Subject

General Materials Science

Link

http://pubs.acs.org/doi/pdf/10.1021/acsami.9b03291

Reference39 articles.

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2. Dehydro coupling of aromatic nuclei by catalyst-oxidant systems: poly(p-phenylene)

3. A NOVEL TYPE OF POLYCONDENSATION OF POLYHALOGENATED ORGANIC AROMATIC COMPOUNDS PRODUCING THERMOSTABLE POLYPHENYLENE TYPE POLYMERS PROMOTED BY NICKEL COMPLEXES

4. Synthesis of polyphenylene from a cis-dihydrocatechol biologically produced monomer

5. Stereoregular Precursors to Poly(p-phenylene) via Transition-Metal-Catalyzed Polymerization. 1. Precursor Design and Synthesis

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