Nickel-Induced Skeletal Rearrangement of Free Base trans-Chlorins into Monofused NiII-Porphyrins: Synthesis, Structural, Spectral, and Electrochemical Redox Properties-Reference-Cited by-同舟云学术

Nickel-Induced Skeletal Rearrangement of Free Base trans-Chlorins into Monofused NiII-Porphyrins: Synthesis, Structural, Spectral, and Electrochemical Redox Properties

Published:2018-09-04 Issue:18 Volume:57 Page:11349-11360
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Chaudhri Nivedita¹,Grover Nitika¹,Sankar Muniappan¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee 247667, India

Funder

Council of Scientific and Industrial Research

Science and Engineering Research Board

Ministry of Human Resource Development

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.8b00798

Reference80 articles.

1. De Novo Synthesis of Gem-Dialkyl Chlorophyll Analogues for Probing and Emulating Our Green World

2. Synthetic Chlorins, Possible Surrogates for Chlorophylls, Prepared by Derivatization of Porphyrins

3. Photosensitizers of the porphyrin and phthalocyanine series for photodynamic therapy

4. Porphyrin-based photosensitizers for use in photodynamic therapy

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