[18]/[20]π Hemiporphyrazine: A Redox-Switchable Near-Infrared Dye-Reference-Cited by-同舟云学术

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[18]/[20]π Hemiporphyrazine: A Redox-Switchable Near-Infrared Dye

Published:2011-12-21 Issue:1 Volume:134 Page:190-193
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Muranaka Atsuya¹²,Ohira Shino¹,Hashizume Daisuke³,Koshino Hiroyuki⁴,Kyotani Fumiko¹,Hirayama Machiko¹,Uchiyama Masanobu¹⁵

Affiliation:

1. Advanced Elements Chemistry Research Team, RIKEN-ASI, Wako-shi, Saitama 351-0198, Japan

2. PRESTO, Japan Science and Technology Agency (JST), 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan

3. Advanced Technology Support Division, RIKEN-ASI, Wako-shi, Saitama 351-0198, Japan

4. Molecular Characterization Team, RIKEN-ASI, Wako-shi, Saitama 351-0198, Japan

5. Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja210410c

Reference30 articles.

1. 976. Conjugated macrocycles. Part XXIV. A new type of cross-conjugated macrocycle, related to the azaporphins

2. Conjugated macrocycles. Part XXV. Cross-conjugated macrocycles with inner great rings of 16, 20, and 24 atoms

3. Phthalocyanine analogues. Part 1. Synthesis, spectroscopy, and theoretical study of 8,18-dihydrodibenzo[b,l]-5,7,8,10,15,17,18,20-octa-azaporphyrin and MNDO calculations on its related Hückel heteroannulene

4. Hemiporphyrazines as Targets for the Preparation of Molecular Materials: Synthesis and Physical Properties

5. Structure, electronic and vibrational spectra and aromaticity of hemiporphyrazine and its hydrates: A density functional theory study

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