Abstract:Ruthenium half-sandwich complexes are central in a wide range of diverse applications in the field of organometallic chemistry. As such, exploration of their preparation and reactivity is crucial for development of their chemistry. Herein, we present alternative synthetic methods for the preparation of Cp*Ru(dppm)Cl, Cp*Ru(dppe)Cl, Cp*Ru(dppf)Cl, [Cp*Ru(COD)(MeCN)]BF4, and [Cp*Ru(bpy)(MeCN)]BF4 (dppm = 1,2-bis(diphenylphosphino)methane; dppe = 1,2-bis(diphenylphosphino) ethane; dppf = 1,2-bis(diphenylphosphino… Show more
“…The compounds 1 , 2 , 5 , 7 , 8 , 9 , 11 , 12 , 13 , 15 , 20 , and Fc[PF 6 ] were synthesized according to existing literature procedures. All other reagents and materials were obtained from commercial suppliers and used as received.…”
To study the switching properties of photochromes, we
undertook
the synthesis and characterization of several ruthenium organometallic
complexes of the type [Ru(Cp*)(dppe)(CC-SP)] or [Ru(CO)(dppe)(PPh3)Cl(CHCH-SP)], where SP = spiropyran. The spectroscopic
and electrochemical properties of the complexes were determined by
careful cyclic voltammetric and spectroelectrochemical experiments.
Whereas the mononuclear alkynyl ruthenium complexes undergo one-electron
oxidations localized over the metal alkynyl moiety, the oxidation
of the mononuclear vinyl ruthenium complexes is centered on the indoline
moiety of the spiropyran. Through these studies, we demonstrate access
to several stable redox states, in addition to switching states attained
via acidochromism and/or photoisomerization.
“…The compounds 1 , 2 , 5 , 7 , 8 , 9 , 11 , 12 , 13 , 15 , 20 , and Fc[PF 6 ] were synthesized according to existing literature procedures. All other reagents and materials were obtained from commercial suppliers and used as received.…”
To study the switching properties of photochromes, we
undertook
the synthesis and characterization of several ruthenium organometallic
complexes of the type [Ru(Cp*)(dppe)(CC-SP)] or [Ru(CO)(dppe)(PPh3)Cl(CHCH-SP)], where SP = spiropyran. The spectroscopic
and electrochemical properties of the complexes were determined by
careful cyclic voltammetric and spectroelectrochemical experiments.
Whereas the mononuclear alkynyl ruthenium complexes undergo one-electron
oxidations localized over the metal alkynyl moiety, the oxidation
of the mononuclear vinyl ruthenium complexes is centered on the indoline
moiety of the spiropyran. Through these studies, we demonstrate access
to several stable redox states, in addition to switching states attained
via acidochromism and/or photoisomerization.
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