[1]
Braun A, Tcherniac J. Über die Produkte der Einwirkung von Acetanhydrid auf Phthalamid. Berichte der deutschen chemischen Gesellschaft, 40 (1907) 2709-2714.
DOI: 10.1002/cber.190704002202
Google Scholar
[2]
Leznoff C C, Lever A B P. Phthalocyanines: properties and applications. New York: VCH, (1989).
Google Scholar
[3]
McKeown N B. Phthalocyanine materials: synthesis, structure, and function. Cambridge University Press, (1998).
Google Scholar
[4]
Kadish K M, Smith K M, Guilard R. The Porphyrin Handbook: Inorganic, organometallic and coordination chemistry. Access Online via Elsevier, (2003).
Google Scholar
[5]
Robertson N. Optimizing Dyes for Dye-Sensitized Solar Cells. Angewandte Chemie International Edition, 45 (2006) 2338-2345.
DOI: 10.1002/anie.200503083
Google Scholar
[6]
Thomas A L. CRC Phthalocyanine Research and Applications. CRC Press, (1990).
Google Scholar
[7]
Nalwa H S. Organometallic materials for nonlinear optics. Applied organometallic chemistry, 5 (1991) 349-377.
DOI: 10.1002/aoc.590050502
Google Scholar
[8]
Nalwa H S. X-Ray photoelectron spectroscopy and electrical conductivity studies of metallophthalocyanine sheet polymers. Applied Organometallic Chemistry, 5 (1991) 203-206.
DOI: 10.1002/aoc.590050310
Google Scholar
[9]
Basova T V, Kolesov B A. Raman polarization studies of the orientation of molecular thin films. Thin Solid Films, 325 (1998) 140-144.
DOI: 10.1016/s0040-6090(98)00485-4
Google Scholar
[10]
George R D, Snow A W, Shirk J S, et al. The alpha substitution effect on phthalocyanine aggregation. Journal of Porphyrins and Phthalocyanines, 2 (1998) 1-7.
DOI: 10.1002/(sici)1099-1409(199801/02)2:1<1::aid-jpp43>3.0.co;2-l
Google Scholar
[11]
Zhao F, Harnisch F, Schröder U, et al. Application of pyrolysed iron (II) phthalocyanine and CoTMPP based oxygen reduction catalysts as cathode materials in microbial fuel cells. Electrochemistry Communications, 7 (2005) 1405-1410.
DOI: 10.1016/j.elecom.2005.09.032
Google Scholar
[12]
Nakazawa T, Nagahashi K, Aizawa T. Photosensitive material for electrophotography having a polyvinyl carbazole derivative, phthalocyanine, and an electron-acceptor.U.S. Patent 4214907. (1980).
Google Scholar
[13]
Kubota L T, Gushikem Y, Perez J, et al. Electrochemical properties of iron phthalocyanine immobilized on titanium (IV) oxide coated on silica gel surface. Langmuir, 11 (1995) 1009-1013.
DOI: 10.1021/la00003a052
Google Scholar
[14]
Ozoemena K I, Nyokong T. Electrocatalytic oxidation and detection of hydrazine at gold electrode modified with iron phthalocyanine complex linked to mercaptopyridine self-assembled monolayer. Talanta, 67 (2005) 162-168.
DOI: 10.1016/j.talanta.2005.02.030
Google Scholar
[15]
Linstead R P. 212. Phthalocyanines. Part I. A new type of synthetic colouring matters. Journal of the Chemical Society (Resumed), (1934) 1016-1017.
DOI: 10.1039/jr9340001016
Google Scholar
[16]
Dent C E, Linstead R P, Lowe A R. 217. Phthalocyanines. Part VI. The structure of the phthalocyanines. Journal of the Chemical Society (Resumed), (1934) 1033-1039.
DOI: 10.1039/jr9340001033
Google Scholar
[17]
Melmed A J, Müller E W. Study of molecular patterns in the field emission microscope. The Journal of Chemical Physics, 29 (1958) 1037.
Google Scholar
[18]
Kluson P, Drobek M, Kalaji A, et al. Preparation, chemical modification and absorption properties of various phthalocyanines. Research on Chemical Intermediates, 35 (2009) 103-116.
DOI: 10.1007/s11164-008-0003-7
Google Scholar
[19]
Parton R F, Neys P E, Jacobs P A, et al. Iron-phthalocyanine immobilized on activated carbon black: a selective catalyst for alkane oxidation. Journal of catalysis, 164 (1996) 341-346.
DOI: 10.1006/jcat.1996.0390
Google Scholar
[20]
Sosa R C, Parton R F, Neys P E, et al. Surface modification of carbon black by oxidation and its influence on the activity of immobilized catalase and iron-phthalocyanines. Journal of Molecular Catalysis A: Chemical, 110 (1996) 141-151.
DOI: 10.1016/1381-1169(96)00197-5
Google Scholar
[21]
Sorokin A B, Tuel A. Metallophthalocyanine functionalized silicas: catalysts for the selective oxidation of aromatic compounds. Catalysis today, 57 (2000) 45-59.
DOI: 10.1016/s0920-5861(99)00312-0
Google Scholar
[22]
Sorokin A B, Kudrik E V. Phthalocyanine metal complexes: versatile catalysts for selective oxidation and bleaching. Catalysis Today, 159 (2011) 37-46.
DOI: 10.1016/j.cattod.2010.06.020
Google Scholar
[23]
Method of preparing metal phthalocyanines from phthalic anhydride and urea. RU Patent 2148582. (2000).
Google Scholar
[24]
Sheljapin O P, Borovkov A G E, Kultaev V N. Method of obtaining metal phthalocyanines from phthalic anhydride. RU Patent 2352571. (2009).
Google Scholar
[25]
Safari N, Jamaat P R, Shirvan S A, et al. Rapid and efficient synthesis of metallophthalocyanines in ionic liquid. Journal of Porphyrins and Phthalocyanines, 9 (2005) 256-261.
DOI: 10.1142/s1088424605000320
Google Scholar
[26]
Shen Y J. Synthesis and application of phthalocyanine. Beijing: Chemical Industry Press, (2000).
Google Scholar
[27]
Edwards L, Gouterman M. Porphyrins: XV. Vapor absorption spectra and stability: Phthalocyanines. Journal of Molecular Spectroscopy, 33 (1970) 292-310.
Google Scholar
[28]
Villemin D, Hammadi M, Hachemi M, et al. Applications of microwave in organic synthesis: an improved one-step synthesis of metallophthalocyanines and a new modified microwave oven for dry reactions. Molecules, 6 (2001) 831-844.
DOI: 10.3390/61000831
Google Scholar