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FacetiousLobster/sandbox
Skeletal formula
Ball-and-stick model
Names
Other names
  • Phthalocyanin
  • Pigment Blue 16
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C32H18N8/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25/h1-16H,(H2,33,34,35,36,37,38,39,40) ☒N
    Key: IEQIEDJGQAUEQZ-UHFFFAOYSA-N ☒N
  • InChI=1S/C32H18N8/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25/h1-16H,(H2,33,34,35,36,37,38,39,40)
    Key: IEQIEDJGQAUEQZ-UHFFFAOYSA-N
  • C12=CC=CC=C1/C3=N/C4=C5C=CC=CC5=C(/N=C6C7=CC=CC=C7C(/N=C8C9=C(/C(N/8)=N/C2=N3)C=CC=C9)=N/6)N4
Properties
C32H18N8
Molar mass 514.552 g·mol−1
Hazards
GHS labelling:
GHS07: Exclamation mark[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tracking categories (test):

Phthalocyanine (H2Pc) is a large, aromatic, macrocyclic, organic compound with the formula (C8H4N2)4H2 and is of theoretical or specialized interest. It is composed of four isoindole units linked by nitrogen atoms. H2Pc has a two-dimensional geometry and a ring system consisting of 18 π-electrons. The extensive delocalization of the π-electrons affords the molecule useful properties, lending itself to applications in dyes and pigments. Metal complexes derived from Pc2−
, the conjugate base of H2Pc, are valuable in catalysis, organic solar cells, and photodynamic therapy.

Properties

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Phthalocyanine and derived metal complexes (MPc) tend to aggregate and, thus, have low solubility in common solvents.[2] Benzene at 40 °C dissolves less than a milligram of H
2Pc or CuPc per litre. H
2Pc and CuPc dissolve easily in sulfuric acid due to the protonation of the nitrogen atoms bridging the pyrrole rings. Many phthalocyanine compounds are, thermally, very stable and do not melt but can be sublimed; CuPc sublimes at above 500 °C under inert gases (nitrogen, CO
2).[3] Substituted phthalocyanine complexes often have much higher solubility.[4] They are less thermally stable and often can not be sublimed. Unsubstituted phthalocyanines strongly absorb light between 600 and 700 nm, thus these materials are blue or green.[2] Substitution can shift the absorption towards longer wavelengths, changing color from pure blue to green to colorless (when the absorption is in the near infrared).

There are many derivatives of the parent phthalocyanine, where either carbon atoms of the macrocycle are exchanged for nitrogen atoms or the peripheral hydrogen atoms are substituted by functional groups like halogens, hydroxyl, amine, alkyl, aryl, thiol, alkoxy and nitrosyl groups. These modifications allow for the tuning of the electrochemical properties of the molecule such as absorption and emission wavelengths and conductance.[5]

History

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In 1907, an unidentified blue compound, now known to be phthalocyanine, was reported.[6] In 1927, Swiss researchers serendipitously discovered copper phthalocyanine, copper naphthalocyanine, and copper octamethylphthalocyanine in an attempted conversion of o-dibromobenzene into phthalonitrile. They remarked on the enormous stability of these complexes but did not further characterize them.[7] In the same year, iron phthalocyanine was discovered at Scottish Dyes of Grangemouth, Scotland (later ICI).[8] It was not until 1934 that Sir Patrick Linstead characterized the chemical and structural properties of iron phthalocyanine.[9]

Synthesis

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Phthalocyanine is formed through the cyclotetramerization of various phthalic acid derivatives including phthalonitrile, diiminoisoindole, phthalic anhydride, and phthalimides.[10] Alternatively, heating phthalanhydride in the presence of urea yields H2Pc.[11] Using such methods, approximately 57,000 tonnes (63,000 tons) of various phthalocyanines were produced in 1985.[11]

STM images of individual phthalocyanine molecules recorded at a bias of −2 V (left) and +1 V (right). Note that STM probes density of electrons in the HOMO/LUMO bands rather than atomic profiles.[12]

More often, MPc is synthesized rather H2Pc due to the greater research interest in the former. To prepare these complexes, the phthalocyanine synthesis is conducted in the presence of metal salts. Two copper phthalocyanines are shown in the figure below. Halogenated and sulfonated derivatives of copper phthalocyanines are commercially important as dyes and pigments. Such compounds are prepared by treating CuPc with chlorine, bromine or oleum.

Applications

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See also: Copper phthalocyanine

At the initial discovery of Pc, its uses were primarily limited to dyes and pigments.[13] Modification of the substituents attached to the peripheral rings allows for the tuning of the absorption and emission properties of Pc to yield differently colored dyes and pigments. There has since been significant research on H2Pc and MPc resulting in a wide range of applications in areas including photovoltaics, photodynamic therapy, nanoparticle construction, and catalysis.[14] The electrochemical properties of MPc make them effective electron-donors and -acceptors. As a result, MPc-based organic solar cells with power conversion efficiencies at or below 5% have been developed.[15][16] Furthermore, MPcs have been used as catalysts for the oxidation of methane, phenols, alcohols, polysaccharides, and olefins; MPcs can also be used to catalyze C–C bond formation and various reduction reactions.[17] Silicon and zinc phthalocyanines have been developed as photosensitizers for non-invasive cancer treatment.[18] Various MPcs have also shown the ability to form nanostructures which have potential applications in electronics and biosensing.[19][20][21]

Toxicity and hazards

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No evidence has been reported for acute toxicity or carcinogenicity of phthalocyanine compounds. The LD50 (rats, oral) is 10 g/kg.[11]

[edit]
Relationship of the phthalocyanine with the porphyrin macrocycle. Two intramacrocyclic N-H groups are omitted.

Phthalocyanines are structurally related to other tetrapyrrole macrocyles including porphyrins and porphyrazines. They feature four pyrrole-like subunits linked to form a 16-membered inner ring composed of alternating carbon and nitrogen atoms. Structurally larger analogues include naphthalocyanines. The pyrrole-like rings within H
2Pc are closely related to isoindole. Both porphyrins and phthalocyanines function as planar tetradentate dianionic ligands that bind metals through four inwardly projecting nitrogen centers. Such complexes are formally derivatives of Pc2−
, the conjugate base of H
2Pc.

References

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  1. ^ Pubchem. "Pigment blue 16". pubchem.ncbi.nlm.nih.gov. Retrieved 2018-04-08.
  2. ^ a b Ghani, Fatemeh; Kristen, Juliane; Riegler, Hans (2012-02-09). "Solubility Properties of Unsubstituted Metal Phthalocyanines in Different Types of Solvents". Journal of Chemical & Engineering Data. 57 (2): 439–449. doi:10.1021/je2010215. ISSN 0021-9568.
  3. ^ Wagner, Hans J.; Loutfy, Rafik O.; Hsiao, Cheng-Kuo (1982-10-01). "Purification and characterization of phthalocyanines". Journal of Materials Science. 17 (10): 2781–2791. doi:10.1007/bf00644652. ISSN 0022-2461.
  4. ^ Nemykin, Victor N.; Lukyanets, Evgeny A. (2010-02-18). "Synthesis of substituted phthalocyanines". Arkivoc. 2010 (1). doi:10.3998/ark.5550190.0011.104.
  5. ^ Siles, P. F.; Hahn, T.; Salvan, G.; Knupfer, M.; Zhu, F.; Zahn, D. R. T.; Schmidt, O. G. (2016-04-21). "Tunable charge transfer properties in metal-phthalocyanine heterojunctions". Nanoscale. 8 (16): 8607–8617. doi:10.1039/c5nr08671j. ISSN 2040-3372.
  6. ^ Braun, A.; Tcherniac, J. (1907). "Über die Produkte der Einwirkung von Acetanhydrid auf Phthalamid" [On the products of the reaction of acetic anhydride with phthalamide]. Berichte der Deutschen Chemischen Gesellschaft. 40 (2). Deutsche Chemische Gesellschaft: 2709–2714. doi:10.1002/cber.190704002202.
  7. ^ De Diesbach, Henri; von Der Weid, Edmond (1927). "Quelques sels complexes des o-dinitriles avec le cuivre et la pyridine" [Certain complex salts of o-dinitriles with copper and pyridine]. Helvetica Chimica Acta. 10: 886. doi:10.1002/hlca.192701001110.
  8. ^ "The Discovery of a New Pigment—The Story of Monastral Blue by Imperial Chemical Industries". colorantshistory.org.
  9. ^ Linstead, R. P. (1934-01-01). "212. Phthalocyanines. Part I. A new type of synthetic colouring matters". Journal of the Chemical Society (Resumed). 0: 1016. doi:10.1039/jr9340001016. ISSN 0368-1769.
  10. ^ Sakamoto, Keiichi; Ohno-Okumura, Eiko (2009-08-28). "Syntheses and Functional Properties of Phthalocyanines". Materials. 2 (3): 1127–1179. doi:10.3390/ma2031127.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  11. ^ a b c Löbbert, Gerd. "Phthalocyanines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a20_213. ISBN 978-3527306732..
  12. ^ Iannuzzi, Marcella; Tran, Fabien; Widmer, Roland; Dienel, Thomas; Radican, Kevin; Ding, Yun; Hutter, Jürg; Gröning, Oliver (2014). "Site-selective adsorption of phthalocyanine on h-BN/Rh(111) nanomesh". Physical Chemistry Chemical Physics. 16 (24): 12374. Bibcode:2014PCCP...1612374I. doi:10.1039/C4CP01466A. PMID 24828002.
  13. ^ Dahlen, Miles A. (1939-07-01). "The Phthalocyanines A New Class of Synthetic Pigments and Dyes". Industrial & Engineering Chemistry. 31 (7): 839–847. doi:10.1021/ie50355a012. ISSN 0019-7866.
  14. ^ Claessens, Christian G.; Hahn, Uwe; Torres, Tomás (2008). "Phthalocyanines: From outstanding electronic properties to emerging applications". The Chemical Record. 8 (2): 75–97. doi:10.1002/tcr.20139. ISSN 1528-0691.
  15. ^ Kumar, Challuri Vijay; Sfyri, Georgia; Raptis, Dimitrios; Stathatos, Elias; Lianos, Panagiotis (2014-12-10). "Perovskite solar cell with low cost Cu-phthalocyanine as hole transporting material". RSC Advances. 5 (5): 3786–3791. doi:10.1039/c4ra14321c. ISSN 2046-2069.
  16. ^ Yuen, Avery P.; Jovanovic, Stephen M.; Hor, Ah-Mee; Klenkler, Richard A.; Devenyi, Gabriel A.; Loutfy, Rafik O.; Preston, John S. (2012). "Photovoltaic properties of M-phthalocyanine/fullerene organic solar cells". Solar Energy. 86 (6): 1683–1688. doi:10.1016/j.solener.2012.03.019.
  17. ^ Sorokin, Alexander B. (2013-10-09). "Phthalocyanine Metal Complexes in Catalysis". Chemical Reviews. 113 (10): 8152–8191. doi:10.1021/cr4000072. ISSN 0009-2665.
  18. ^ MILLER, J; BARON, E; SCULL, H; HSIA, A; BERLIN, J; MCCORMICK, T; COLUSSI, V; KENNEY, M; COOPER, K (2007). "Photodynamic therapy with the phthalocyanine photosensitizer Pc 4: The case experience with preclinical mechanistic and early clinical–translational studies". Toxicology and Applied Pharmacology. 224 (3): 290–299. doi:10.1016/j.taap.2007.01.025.
  19. ^ Karan, Santanu; Basak, Dhrubajyoti; Mallik, Biswanath (2007). "Copper phthalocyanine nanoparticles and nanoflowers". Chemical Physics Letters. 434 (4–6): 265–270. doi:10.1016/j.cplett.2006.12.007.
  20. ^ Van Keuren, Edward; Bone, Alysia; Ma, Changbao (2008-06-01). "Phthalocyanine Nanoparticle Formation in Supersaturated Solutions". Langmuir. 24 (12): 6079–6084. doi:10.1021/la800290s. ISSN 0743-7463.
  21. ^ Lokesh, K.S.; Shivaraj, Y.; Dayananda, B.P.; Chandra, Sudeshna (2009). "Synthesis of phthalocyanine stabilized rhodium nanoparticles and their application in biosensing of cytochrome c". Bioelectrochemistry. 75 (2): 104–109. doi:10.1016/j.bioelechem.2009.02.005.
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