Triphenyl borates used to avoid the bay-position halogenation of boron subnaphthalocyanines; and for the subnaphthalocyanine, subphthalocyanine and hybrids formation-Reference-Cited by-同舟云学术

Triphenyl borates used to avoid the bay-position halogenation of boron subnaphthalocyanines; and for the subnaphthalocyanine, subphthalocyanine and hybrids formation

Published:2024 Issue:12 Volume:48 Page:5127-5143
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Holst Devon P.¹^ORCID,Dovijarski Aleksa¹^ORCID,Lough Alan J.¹,Bender Timothy P.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario, M5S 3H6, Canada

2. Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College Street, Toronto, Ontario, M5S 3E5, Canada

3. Department of Materials Science and Engineering, University of Toronto, 184 College Street, Toronto, Ontario, M5S 3E4, Canada

4. Department of Mechanical and Industrial Engineering, University of Toronto, 5 King's College Road, Toronto, Ontario, M5S 3G8, Canada

Abstract

Avoiding the random bay-position halogenation of boron subnapthalocyanines and to balance of Lewis's acidity and basicity to enable the formation.

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NJ/D4NJ00115J

Reference78 articles.

1. Boron Subphthalocyanines as Organic Electronic Materials

2. Pentafluorophenoxy Boron Subphthalocyanine As a Fluorescent Dopant Emitter in Organic Light Emitting Diodes

3. Fluorinated Phenoxy Boron Subphthalocyanines in Organic Light-Emitting Diodes

4. 8.4% efficient fullerene-free organic solar cells exploiting long-range exciton energy transfer

5. n-Channel Organic Field-Effect Transistors Based on Boron-Subphthalocyanine

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