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Usp. Khim., 2011, Volume 80, Issue 6, Pages 558–579 (Mi rcr59)  

This article is cited in 11 scientific papers (total in 11 papers)

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

A. Yu. Tolbina, L. G. Tomilovaba

a Institute of Physiologically Active Compounds RAS, Chernogolovka
b Lomonosov Moscow State University, Faculty of Chemistry

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.

Full text: http://www.uspkhim.ru/.../paper_rus.phtml?journal_id=rc&paper_id=4198

English version:
Russian Chemical Reviews, 2011, 80:6, 531–551

Bibliographic databases:

Document Type: Article
Received: 24.11.2010

Citation: A. Yu. Tolbin, L. G. Tomilova, “Subphthalocyanines and their analogues: methods for the synthesis and structure modification”, Usp. Khim., 80:6 (2011), 558–579; Russian Chem. Reviews, 80:6 (2011), 531–551

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    Citing articles on Google Scholar: Russian citations, English citations
    Related articles on Google Scholar: Russian articles, English articles

    This publication is cited in the following articles:
    1. A. Yu. Tolbin, L. G. Tomilova, “ChemInform Abstract: Subphthalocyanines and Their Analogues: Methods for the Synthesis and Structure Modification”, ChemInform, 42:50 (2011), no  crossref
    2. Graham E. Morse, Timothy P. Bender, “Boron Subphthalocyanines as Organic Electronic Materials”, ACS Appl. Mater. Interfaces, 2012, 1209271310  crossref  isi  scopus
    3. Kumar A., Debnath A.K., Samanta S., Singh A., Prasad R., Veerender P., Singh S., Basu S., Aswal D.K., Gupta S.K., “Enhanced Cl-2 Response of Ultrathin Bi-Nuclear (Cobalt-Iron) Phthalocyanine Films”, Sens. Actuator B-Chem., 171 (2012), 423–430  crossref  isi  scopus
    4. Ch.G.. Claessens, David González-Rodríguez, M. Salomé Rodríguez-Morgade, Anaïs Medina, Tomás Torres, “Subphthalocyanines, Subporphyrazines, and Subporphyrins: Singular Nonplanar Aromatic Systems”, Chem. Rev, 2013, 1312190932  crossref  isi  scopus
    5. Viswanath L.C.K., Shirtcliff L.D., Berlin K.D., “Synthesis of Symmetrical and Unsymmetrical Subphthalocyanine Dimers Containing a Hydroquinone Bridge”, J. Porphyr. Phthalocyanines, 17:12 (2013), 1167–1172  crossref  isi  elib  scopus
    6. Belen'kii L.I. Evdokimenkova Yu.B., “The Literature of Heterocyclic Chemistry, Part XII, 2010-2011”, Advances in Heterocyclic Chemistry, Vol 111, Adv. Heterocycl. Chem., 111, ed. Katritzky A., 2014, 147–274  crossref  isi  scopus
    7. Dubinina T.V., Osipova M.M., Zasedatelev A.V., Krasovskii V.I., Borisova N.E., Trashin S.A., Tomilova L.G., Zefirov N.S., “Synthesis, optical and electrochemical properties of novel phenyl- and phenoxy-substituted subphthalocyanines”, Dyes Pigment., 128 (2016), 141–148  crossref  isi  scopus
    8. Shvedene N.V., Otkidach K.N., Ondar E.E., Osipova M.M., Dubinina T.V., Tomilova L.G., Pletnev I.V., “Phenoxy-substituted boron subphthalocyanine as a ionophore of ion-selective electrodes”, J. Anal. Chem., 72:1 (2017), 95–104  crossref  isi  scopus
    9. Gonzalez-Anton R., Osipova M.M., Garcia-Hernandez C., Dubinina T.V., Tomilova L.G., Garcia-Cabezon C., Rodriguez-Mendez M.L., “Subphthalocyanines as Electron Mediators in Biosensors Based on Phenol Oxidases: Application to the Analysis of Red Wines”, Electrochim. Acta, 255 (2017), 239–247  crossref  isi  scopus
    10. Bernhard Ya., Richard Ph., Decreau R.A., “Addressing Subphthalocyanines and Subnaphthalocyanines Features Relevant to Fluorescence Imaging”, Tetrahedron, 74:10 (2018), 1047–1052  crossref  isi  scopus
    11. Shvedene N.V., Abashev M.N., Arakelyan S.A., Otkidach K.N., Tomilova L.G., Pletnev I.V., “Highly Selective Solid-State Sensor For Iodide Based on the Combined Use of Platinum (Iv) Phthalocyanine and Solidified Pyridinium Ionic Liquid”, J. Solid State Electrochem., 23:2 (2019), 543–552  crossref  isi  scopus
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