NDLI: Photochemical behavior of (diphosphine)(η $^{2}-tolane)Pt$ $^{0}$ complexes. Part A: Experimental considerations in solution and in the solid state

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Görls, Helmar Petzold, Holm Weisheit, Thomas Escudero, Daniel Weigand, Wolfgang González, Leticia
Description	Author Affiliation: Weisheit T ( Institut für Anorganische und Analytische Chemie, Friedrich-Schiller-Universität Jena, August-Bebel-Str. 2, 07743, Jena, Germany.)
Abstract	A series of various (diphosphine)(η $^{2}-tolane)Pt$ $^{0}$ complexes exhibiting manifold substitution pattern of the tolane ligand (5a–g) and different rigid diphosphines defining various bite angles at the Pt center (9a–b) have been synthesized. All compounds were isolated and characterized by means of spectroscopic methods and additionally by X-ray structure determination (5a–e, 9a–b). In view of potential $C_{aryl}–$ C $_{ethynyl}$ bond activation , we investigated their photochemical behavior in the solid state as well as in solution by irradiating with sunlight. The reactivity towards $C_{aryl}–$ C $_{ethynyl}$ bond activation in the crystalline state and in solution is discussed in relation to substituents attached to the tolane ligand and on the extent of the torsion of its phenyl rings. Complexes 5a–c and 9a either bearing electron withdrawing bromides or possessing a large dihedral angle of the phenyl rings, showed selective oxidative addition of the $C_{aryl}–$ C $_{ethynyl}$ bond to the Pt center in the solid state, yielding complexes 6a–c and 10a, respectively. In contrast, 5d–f and 9b proved to be unreactive under similar conditions because of their electron donating methoxy groups as well as the reduced twisting of their phenyl or pyridyl moieties of the tolane ligands. Irradiation of complexes 5a and 5b with sunlight in solution revealed the formation of the appropriate C–Br activated compounds 7a and 7b along with 6a and 6b in a 1:1 mixture. The observed photochemical $C_{aryl}–$ C $_{ethynyl}$ bond activation is reversible under thermal conditions, regaining the appropriate Pt $^{0}$ complexes by reductive elimination.
ISSN	14779226
Issue Number	40
Journal	Dalton Trans.
Volume Number	39
e-ISSN	13645447
Language	English
Publisher	Royal Society of Chemistry
Publisher Date	2010-10-28
Publisher Place	Great Britain (UK)
Access Restriction	Subscribed
Subject Keyword	Chemistry
Content Type	Text
Resource Type	Article
Subject	Inorganic Chemistry

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