Phthalocyanine

Phthalocyanine CAS: 574-93-6 MDL: MFCD00005085

Molecular weight: 514.54 g/mol

Molecular Formula: C₃₂H₁₈N₈

CAS Number: 574-93-6

Storage: Store at room temperature, protect from light.

Synonyms: (2Z)-2,11,20,29,37,38,39,40-Octaazanonacyclo[28.6.1.1^3,10.1^12,19.1^21,28.0^4,9.0^13,18.0^22,27.0^31,36]tetraconta-1(37),2,4,6,8,10(40),11,13,15,17,19(39),21,23,25,27,29,31,33,35-nonadecaene, 2,11,20,29,37,38,39,40-octaazanonacyclo[28.6.1.1³,¹?.1¹²,¹?.1²¹,²?.0?,?.0¹³,¹?.0²²,²?.0³¹,³?]tetraconta-1,3,5,7,9,11,13(18),14,16,19(39),20,22(27),23,25,28,30(37),31(36),32,34-nonadecaene, 209-378-3, 29H,30H-Phthalocyanin, 29H,30H-Phthalocyanine, 29H,30H-Phthalocyanine, 29H,31H-Phthalocyanine, 29H,31H-Phthalocyanine, 378323, 5,28-Dihydro-29H,31H-phthaloCyanine, 521983-41-5, 574-93-6, 6H,30H-Phthalocyanine, 6H,30H-Phthalocyanine, CI Pigment Blue 16, Colour Index, Pigment Blue 16, MFCD00005085, MICA, Phthalocyanine, Pigment blue 16, V5PUF4VLGY, 162831-66-5, 2,11,20,29,37,38,39,40-Octazanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3(40),4,6,8,10,12(39),13,15,17,19,21,23,25,27,30(37),31,33,35-nonadecaene, 2612-54-6, 29H, 31H-Phthalocyanine, 31H-phthalocyanine, 4466-64-2, 5,28:14,19-Diimino-7,12:26,21-dinitrilotetrabenzo(c,h,m,r)(1,6,11,16)tetraazacycloeicosine, 52440-51-4, 81612-16-0, ftalocianina, Heliogen Blue 7560, Heliogen Blue 7800, Heliogen Blue G, Irgazin Blue 3GT, Lionol Blue KW, Monolite Fast Blue GS, Phthalocyanin, Phthalozyanin, Pigment Blue Green Phthalocyanine U, Polymon Blue G, Tetrabenzo(b,g,l,q)porphyrazine, TETRABENZOPORPHYRAZINE, UNII:V5PUF4VLGY, UNII-V5PUF4VLGY

Fields of Interest: Freebase Phthalocyanines, Pigments, Ligands

Background: Phthalocyanine is a phthalocyanine specialty chemical manufactured by Frontier Specialty Chemicals.

References:

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2.) Wu, et al. Domino electroreduction of CO2 to methanol on a molecular catalyst. Nature, 2019, vol. 575, # 7784, p. 639 – 642. https://doi.org/10.1038/s41586-019-1760-8

3.) Zhang, et al. Efficient Oxygen Reduction Reaction (ORR) Catalysts Based on Single Iron Atoms Dispersed on a Hierarchically Structured Porous Carbon Framework. Angewandte Chemie – International Edition, 2018, vol. 57, # 29, p. 9038 – 9043. https://doi.org/10.1002/anie.201804958

4.) Gregory, et al. Industrial applications of phthalocyanines. Journal of Porphyrins and Phthalocyanines, 2000, vol. 4, # 4, p. 432 – 437. https://doi.org/10.1002/(SICI)1099-1409(200006/07)4:4<432::AID-JPP254>3.0.CO;2-N

5.) Turek, et al. A New Series of Molecular Semiconductors: Phthalocyanine Radicals. Journal of the American Chemical Society, 1987, vol. 109, # 17, p. 5119 – 5122. https://doi.org/10.1021/ja00251a012

6.) Wang, et al. CO₂ electrochemical catalytic reduction with a highly active cobalt phthalocyanine. Nature Communications, 2019, vol. 10, # 1, art. no. 3602. https://doi.org/10.1038/s41467-019-11542-w