Revisiting the intense NIR active bronzaphyrin, a 26-π aromatic expanded porphyrin: synthesis and structural analysis-Reference-Cited by-同舟云学术

Revisiting the intense NIR active bronzaphyrin, a 26-π aromatic expanded porphyrin: synthesis and structural analysis

Published:2018 Issue:93 Volume:54 Page:13135-13138
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Kishore M. V. Nanda¹²³⁴,Panda Pradeepta K.¹²³⁴^ORCID

Affiliation:

1. School of Chemistry

2. University of Hyderabad

3. Hyderabad-500046

4. India

Abstract

The first solid state structural elucidation done for bronzaphyrins via a new dithia-analogue reveals inversion of their thiophene rings, and crystal packing reveals four open dimeric trifluoroacetate [(CF₃COO)₂H]⁻ moieties binding to the macrocycle in its protonated form via H bonding.

Funder

Science and Engineering Research Board

University Grants Commission

Department of Science and Technology, Ministry of Science and Technology

Council of Scientific and Industrial Research

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/2018/CC/C8CC07752E

Reference65 articles.

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4. Novel expanded porphyrin sensitized solar cells using boryl oxasmaragdyrin as the sensitizer

5. Comparative Photophysics of [26]- and [28]Hexaphyrins(1.1.1.1.1.1): Large Two-Photon Absorption Cross Section of Aromatic [26]Hexaphyrins(1.1.1.1.1.1)

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