Influence of the diamine on the reactivity of thiosulfonato ruthenium complexes with hydrosulfide (HS−)
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2013/DT/C2DT31758C
Reference24 articles.
1. An Alternate Route to Disulfanido Complexes by Nucleophilic Attack of Thiolates on Ruthenium-Bound Thiosulfonato Ligands
2. Hydrosulfido complexes of transition metals
3. Interconversion of persulfido, sulfur hydride, and hydride ligands coordinated to CpRu(PPh3)2+
4. Synthesis of cuboidal (C5H4Me)4Ru4E4 by condensation of (C5H4Me)Ru(PPh3)2EH (E = S, Se)
5. Preparation of the thiosulfinato complexes CpRu(PPh3)(CO)SS(O)R, where R = C3H7, CHMe2, and 4-C6H4Me, and the structure for R = CHMe2. Oxygen transfer to give the thiosulfonato complex CpRu(PPh3)(CO)SS(O)2-4-C6H4Me and its structure
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1. Bismuth(III) Complex of the [S4]•– Radical Anion: Dimer Formation via Pancake Bonds;Journal of the American Chemical Society;2017-11-07
2. Sulfur versus Dioxygen: Dinuclear (Trisulfido)copper Complexes;European Journal of Inorganic Chemistry;2016-07
3. Organometallic sulfur complexes: reactivity of the hydrogen sulfide anion with cobaloximes;New Journal of Chemistry;2015
4. Selective P4 activation by an organometallic nickel(i) radical: formation of a dinuclear nickel(ii) tetraphosphide and related di- and trichalcogenides;Chem. Commun.;2014
5. Studies of Iron(III) Porphyrinates Containing Silanethiolate Ligands;Inorganic Chemistry;2013-10-18
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