Literature DB >> 21294748

Solvent dependence of the photophysical properties of 2-chlorothioxanthone, the principal photoproduct of chlorprothixene.

Luis E Piñero Santiago1, Carmelo García, Virginie Lhiaubet-Vallet, Miguel A Miranda, Rolando Oyola.   

Abstract

2-chlorothioxanthone (CTX) is used as photoinitiator for the reticulation of synthetic resins and for the preparation of pharmaceuticals. It was previously determined that CTX is the primary photoproduct of z-chlorprothixene (CPTX) when irradiated at 313 nm and is formed in an autocatalyzed reaction through an energy-transfer mechanism (Piñero et al. [2009] Photochem. Photobiol., 85, 895-900). In this work, the photophysical properties of CTX were measured in acetonitrile/water solutions to determine if their magnitude can affect the side effects of CPTX. The results show that CTX has higher absorption coefficients in the visible region (400-420 nm) and higher triplet quantum yields than its parent compound. Similar to TX, both properties strongly depend on the solvent polarity/hydroxylicity. The quantum yield of the triplet intermediate is very close to the value of the phenothiazine triplets. The phenothiazines are the most phototoxic antidepressants. Therefore, given the appropriate microenvironment, the photosensitization side effects of CPTX can be intensified on the production of CTX.
© 2011 U.S. Government Photochemistry and Photobiology © 2011 The American Society of Photobiology.

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Year:  2011        PMID: 21294748      PMCID: PMC3082582          DOI: 10.1111/j.1751-1097.2011.00906.x

Source DB:  PubMed          Journal:  Photochem Photobiol        ISSN: 0031-8655            Impact factor:   3.421


  17 in total

1.  On the pharmacokinetics of chlorprothixene in man.

Authors:  J Raaflaub
Journal:  Experientia       Date:  1975-05-15

Review 2.  Laser techniques in the study of drug photochemistry.

Authors:  Gonzalo Cosa; J C Scaiano
Journal:  Photochem Photobiol       Date:  2004 Sep-Oct       Impact factor: 3.421

3.  Photodegradation of 2-chloro substituted phenothiazines in alcohols.

Authors:  Carmelo García; Luis Piñero; Rolando Oyola; Rafael Arce
Journal:  Photochem Photobiol       Date:  2008-07-30       Impact factor: 3.421

4.  Ultrafast decay of the excited singlet states of thioxanthone by internal conversion and intersystem crossing.

Authors:  Gonzalo Angulo; Jakob Grilj; Eric Vauthey; Luis Serrano-Andrés; Oscar Rubio-Pons; Patrice Jacques
Journal:  Chemphyschem       Date:  2010-02-01       Impact factor: 3.102

5.  The photochemical stability of cis- and trans-isomers of tricyclic neuroleptic drugs.

Authors:  A Li Wan Po; W J Irwin
Journal:  J Pharm Pharmacol       Date:  1980-01       Impact factor: 3.765

6.  Substitution and solvent effects on the photophysical properties of several series of 10-alkylated phenothiazine derivatives.

Authors:  Carmelo García; Rolando Oyola; Luis E Piñero; Rafael Arce; Jenny Silva; Vicente Sánchez
Journal:  J Phys Chem A       Date:  2005-04-21       Impact factor: 2.781

7.  Photoproducts of chlorpromazine which cause red blood cell lysis.

Authors:  I E Kochevar; J Hom
Journal:  Photochem Photobiol       Date:  1983-02       Impact factor: 3.421

8.  Photoaddition to DNA by nonintercalated chlorpromazine molecules.

Authors:  I E Kochevar; C Garcia; N E Geacintov
Journal:  Photochem Photobiol       Date:  1998-11       Impact factor: 3.421

9.  Spectral and photophysical properties of thioxanthone in protic and aprotic solvents: the role of hydrogen bonds in S1-thioxanthone deactivation.

Authors:  Ewa Krystkowiak; Andrzej Maciejewski; Jacek Kubicki
Journal:  Chemphyschem       Date:  2006-03-13       Impact factor: 3.102

10.  Phenothiazine phototoxicity: an experimental study on chlorpromazine and its metabolites.

Authors:  B Ljunggren; H Möller
Journal:  J Invest Dermatol       Date:  1977-05       Impact factor: 8.551

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