| Name | Cl 6 |
|---|---|
| Synonyms | CD158B; MHC class I NK cell receptor; NKAT; p58 NK receptor; CD158B2; CD158b antigen; CL 6; GL183… |
| Name | phosphine |
|---|---|
| CAS | phosphine |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 15926840 | Balasubramanian R, Guo R, Mills AJ, Murray RW: Reaction of Au (55)(PPh (3))(12) Cl (6) with thiols yields thiolate monolayer protected Au (75) clusters. J Am Chem Soc. 2005 Jun 8;127(22):8126-32. This paper describes the reaction of the phosphine-protected Au nanoparticle Au (55)(PPh (3))(12) Cl (6) (1, "Au55") with hexanethiol (2) and other thiols. |
7(0,0,1,2) | Details |
| 16706449 | Hakkinen H, Walter M, Gronbeck H: Divide and protect: capping gold nanoclusters with molecular gold-thiolate rings. J Phys Chem B. 2006 May 25;110(20):9927-31. Density functional theory calculations are used to explore phosphine- and thiolate-protected gold nanoclusters, namely, Au (39)(PH (3))(14) Cl (6) and Au (38)(SCH (3))(24). |
6(0,0,1,1) | Details |
| 17117219 | Moxham GL, Douglas TM, Brayshaw SK, Kociok-Kohn G, Lowe JP, Weller AS: The role of halogenated carborane monoanions in olefin hydrogenation catalysed by cationic iridium phosphine complexes. Dalton Trans. 2006 Dec 14;(46):5492-505. Epub 2006 Oct 17. Iridium hydridophosphine complexes of general formula [Ir (PR3) 2H2 (anion)](PR3= PPh3, PMe2Ph; anion =[1-closo-CB (11) H (6) Cl (6)]-, [1-closo-CB (11) H (6) I (6)]-, [BAr (F) 4]-) have been prepared by hydrogenation of cyclooctadiene precursor complexes. |
3(0,0,0,3) | Details |
| 16749823 | Matkovich KM, Thorne LM, Wolf MO, Pace TC, Bohne C, Patrick BO: Luminescence of ruthenium halide complexes containing a hemilabile phosphine pyrenyl ether ligand. Inorg Chem. 2006 Jun 12;45(12):4610-8. Complexes 3-5 react rapidly with CO to give complexes ttt-RuX2 (CO) 2 (POC4pyr-P) 2 (X = Cl (6), Br (7), I (8)). |
1(0,0,0,1) | Details |
| 17378566 | Albrecht C, Schwieger S, Bruhn C, Wagner C, Kluge R, Schmidt H, Steinborn D: Alkylthio bridged 44 cve triangular platinum clusters: synthesis, oxidation, degradation, ligand substitution, and quantum chemical calculations. J Am Chem Soc. 2007 Apr 18;129(15):4551-66. Epub 2007 Mar 23. The analogous reaction of 2a-b with Ph2S2 gave SPh bridged dinuclear complexes trans-[{PtCl (L)}2 (mu-SPh) 2] (5), whereas the addition of Bn2S2 (Bn = benzyl) to 2a ended up in the formation of [{Pt (PPh3)}3 (mu3-S)(mu-SBn) 3] Cl (6). Phosphine ligands with a lower donor capability in clusters 4 proved to be subject to substitution by stronger donating monodentate phosphine ligands (L' = PMePh2, PMe2Ph, PBu3) yielding clusters [(PtL') 3 (mu-SR) 3] Cl (9). |
1(0,0,0,1) | Details |
| 16075115 | Novio F, Mas-Balleste R, Gallardo I, Gonzalez-Duarte P, Lledos A, Vila N: Influence of the terminal ligands on the redox properties of the {Pt2 (mu-S) 2} core in [Pt2 (Ph2X (CH2) 2XPh2) 2 (mu-S) 2] (X = P or As) complexes and on their reactivity towards metal centres, protic acids and organic electrophiles. Dalton Trans. 2005 Aug 21;(16):2742-53. Epub 2005 Jul 11. Complex 1 as well as the corresponding multimetallic derivatives [Pt (dpae){Pt2 (dpae) 2 (mu-S) 2}](BPh4) 2 2, [M{Pt2 (dpae) 2 (mu-S) 2}2] X2 (M = Cu (II), X = BF4 3; M = Zn (II), X = BPh4 4; M = Cd (II), X = ClO4 5; M = Hg (II), X = Cl 6 or X2 = Cl (1.5)[HCl2](0.5) 6') have been characterized in the solid phase and in solution. Comparison of structural parameters of 1 and 3-6' with those of the corresponding phosphine analogues, together with the results of the electrochemical study for 1, allow us to conclude that replacement of dppe by dpae causes a decrease in basicity of the {Pt2 (mu-S) 2} core. |
1(0,0,0,1) | Details |