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Subphthalocyanines and their analogues: methods for the synthesis and structure modification

Alexander Yurevich Tolbin 1
Alexander Yurevich Tolbin
, 
Larisa Godvigovna Tomilova 1, 2
Larisa Godvigovna Tomilova
1 Institute of Physiologically Active Compounds RAS, Chernogolovka
2 Lomonosov Moscow State University, Faculty of Chemistry
10.1070/RC2011v080n06ABEH004198
Published 30 November 2010
Communication , Volume 80, Issue 6, 531-551
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Tolbin A. Y., Tomilova L. G. Subphthalocyanines and their analogues: methods for the synthesis and structure modification // Russian Chemical Reviews. 2011. Vol. 80. No. 6. pp. 531-551.
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Tolbin A. Y., Tomilova L. G. Subphthalocyanines and their analogues: methods for the synthesis and structure modification // Russian Chemical Reviews. 2011. Vol. 80. No. 6. pp. 531-551.
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TY - JOUR
DO - 10.1070/RC2011v080n06ABEH004198
UR - https://rcr.colab.ws/publications/10.1070/RC2011v080n06ABEH004198
TI - Subphthalocyanines and their analogues: methods for the synthesis and structure modification
T2 - Russian Chemical Reviews
AU - Tolbin, Alexander Yurevich
AU - Tomilova, Larisa Godvigovna
PY - 2011
DA - 2010/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 531-551
IS - 6
VL - 80
ER -
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@article{2011_Tolbin,
author = {Alexander Yurevich Tolbin and Larisa Godvigovna Tomilova},
title = {Subphthalocyanines and their analogues: methods for the synthesis and structure modification},
journal = {Russian Chemical Reviews},
year = {2011},
volume = {80},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC2011v080n06ABEH004198},
number = {6},
pages = {531--551},
doi = {10.1070/RC2011v080n06ABEH004198}
}
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Tolbin, Alexander Yurevich, and Larisa Godvigovna Tomilova. “Subphthalocyanines and their analogues: methods for the synthesis and structure modification.” Russian Chemical Reviews, vol. 80, no. 6, Nov. 2011, pp. 531-551. https://rcr.colab.ws/publications/10.1070/RC2011v080n06ABEH004198.
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Abstract

Methods for the preparation and modification of mononuclear (A3 and A2B-types) and planar bi- and trinuclear subphthalocyanines are considered. Structural analogues of subphthalocyanines, viz., subazaporphyrins, are also discussed.