Synthesis and Characterisation of Low-Coordinate Transition-Metal Complexes Stabilised by Sterically Demanding Carbazolido Ligands

2009 ◽  
Vol 2009 (17) ◽  
pp. 2547-2552 ◽  
Author(s):  
Andrew E. Ashley ◽  
Andrew R. Cowley ◽  
Jennifer C. Green ◽  
David R. Johnston ◽  
David J. Watkin ◽  
...  
1987 ◽  
Vol 42 (10) ◽  
pp. 1291-1297 ◽  
Author(s):  
Dieter Sellmann ◽  
Olaf Käppler

Abstract In order to obtain soluble complexes containing sterically protected metal centers the new bi- and tetradentate thiolate amine ligands 2-mercapto-3,5-di-tbutylaniline (= tbu2-ma-H) and 1,2-bis(2-mercapto-3,5-di-tbutylanilino)ethane (= tbu4-mae-H2) were synthesized. tbu2-ma-H reacts with FeCl2-4 H2O and CO to give [Fe(CO)2(tbu2-ma)2], with Zn(ac)2 -2 H2O [Zn(tbu2-ma)2] is obtained whose acid hydrolysis and reaction with H2S, respectively, yield pure tbu2-Ina-H. The condensation of tbu2-ma-H with glyoxal yields the respective bis-benzthiazolidine, which is re­duced by LiAlH4 in the presence of Na[N(SiMe3)2] to tbu4-bmae-H2. tbu4-bmae-Li2. reacts with [Ru(CO)3(THF)Cl2], [Ru(PMe3)4Cl2] and [Ru(PPh3)2(CH3CN)2Cl2], respectively, to yield [Ru(L)2(Tm4-bmae)j (L = CO, PMe3, PPh3). The complexes are more soluble in organic solvents than the corresponding unsubstituted bmae complexes, bmae2- = 1,2-bis(2-mercaptoanilino)- ethane(2-).


1995 ◽  
Vol 50 (8) ◽  
pp. 1229-1244 ◽  
Author(s):  
Dieter Sellmann ◽  
Christine Rohm ◽  
Matthias Moll ◽  
Falk Knoch

In a search of transition metal complexes with sulfur dominated coordination spheres and free coordination sites for the binding of small molecules, [Ru(L)('buS5')] complexes with the sterically demanding pentadentate thioether-thiolate ligand 'buS5'2- ( 'buS5'2- = 2,2'-Bis(2-mercapto-3,5-di-t-butylphenylthio)diethylsulfide(2-)) have been synthesized. Reaction of [RuCl3(NO)(PPh3)2] with 3,5-di(t-butyl)benzene-1,2-dithiolate, ′buS2'2-, yields the 16 electron complex [Ru(NO )('buS2')2]- which is isolated as the NBu4+-salt, 1. According to the NMR spectra, 1 contains a two-fold axis or a mirror plane. Alkylation of 1 with bis(β-bromethyl)sulfide under reflux leads stereoselectively to meso-[Ru(NO)('buS5')]Br, [2]Br. Reaction of [2]Br with LiBEt3H yields the barely soluble binuclear complex [Ru('buS5')]2, 3, with [Ru('buS5')Ru(NO)('buS2')('buS2'- C2H4SH)], 4, as a by-product. 4 ·THF, 4a, has been characterized by X-ray structure analysis. Reactions of 3 with σ-π- and σ-ligands yield mononuclear meso-[Ru(L)('buS5')] complexes which have been isolated and characterized with L = CO, PMe3, PPh3, PCy3, pyr, CN-, 5 - 10, NH2NHPh, NH2NHMe, NH2NMe2, NH2Ph und NHEt2, 13-17. Complexes 5 -10 are stable compounds. Complexes 13-17, however, are sensitive towards oxidation and/or substitution. Coordination of L = N2H4 and NH3 to 3 leads to insoluble [Ru(L)('buS5')]x complexes.


2013 ◽  
Vol 52 (19) ◽  
pp. 11126-11135 ◽  
Author(s):  
Keith Searles ◽  
Ba L. Tran ◽  
Maren Pink ◽  
Chun-Hsing Chen ◽  
Daniel J. Mindiola

2019 ◽  
Vol 48 (26) ◽  
pp. 9617-9624 ◽  
Author(s):  
Dae Young Bae ◽  
Gyeong Su Park ◽  
Nakeun Ko ◽  
Kyung-sun Son ◽  
Eunsung Lee

A highly sterically demanding amino triphenolate ligand was successfully synthesized, and early transition metal complexes (Ti, V, Cr, and Mn) supported by the ligand were also obtained and fully characterized.


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