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Abstract
Dinuclear Pd(II) halides that contain bridging π-conjugated groups, trans,trans-[(PR3)2(X)Pd–Y–Pd(X)(PR3)2] (X = Br; YH2 = terpyridine, fluorenone, benzil, benzthiadiazole), were prepared by the oxidative addition of corresponding dihalo π-conjugated reagents to [Pd(styrene)(PR3)2]. Similar reactions involving dihalobenzil, dihalobithiophene, or dihaloterthiophene afforded dinuclear Pt(II) halides containing bridging π-conjugated groups. Additionally, when the dihalosilole derivatives {2,5-dibromo-1,1-dimethyl (or diphenyl)-3,4-diphenylsilole} reacted with [Pd(styrene)(PR3)2], mono or dinuclear Pd(II) complexes bearing a dimethyl (or diphenyl)-3,4-diphenylsilole group were obtained. π-Conjugation extension reactions of dinuclear bithiophene-bridged Pd(II) halides with HC≡C–R {R = SiPh3, C(O)OMe} in the presence of CuI and HNEt2 led to the unexpected formation of bis(acetylide) Pd(II) complexes of the form, [Pd(C≡C–R)2(PR3)2] and bithiophene. In contrast, treatment of the dinuclear Pd(II) halides with two equiv of organic isocyanide resulted in isocyanide insertion into the Pd − C bonds to afford π-conjugation-extended dinuclear Pd(II) compounds bearing a π-conjugated moiety.
Graphical Abstract
Acknowledgement
This work was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (NRF-2016R1D1A3B03932228).
Disclosure statement
No potential conflict of interest was reported by the authors.
Supplementary data
CCDC 1821938 and 1821939 contain the supplementary crystallographic data for this article. Copies of this information may be obtained free of charge from the Director, CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK (Fax: +44-1223-336-033; E-mail: [email protected] or www: http://www.ccdc.cam.ac.uk).