The preparation and coordination chemistry of substituted benzenethiols. Triphenylphosphine gold(I)complexes of sterically demanding and nondemandingarenethiols. The absence of gold(I)–gold(I) interactions

Polyhedron ◽  
1998 ◽  
Vol 18 (3-4) ◽  
pp. 593-600 ◽  
Author(s):  
Laila S. Ahmed ◽  
William Clegg ◽  
Dominic A. Davies ◽  
Jonathan R. Dilworth ◽  
Mark R.J. Elsegood ◽  
...  
2008 ◽  
Vol 27 (4) ◽  
pp. 576-593 ◽  
Author(s):  
Lucas R. Moore ◽  
Elizabeth C. Western ◽  
Raluca Craciun ◽  
Jason M. Spruell ◽  
David A. Dixon ◽  
...  

2016 ◽  
Vol 72 (11) ◽  
pp. 806-812 ◽  
Author(s):  
Yi Rong ◽  
David Sambade ◽  
Gerard Parkin

Cyclopentadienyl and tris(pyrazolyl)hydroborate have found much use as supporting ligands in the chemistry of titanium, zirconium and hafnium, especially with respect to applications involving olefin polymerization catalysis. In contrast, closely related tris(1-alkyl-2-mercaptoimidazolyl)hydroborate, [TmR], ligands have so far found little application to the chemistry of these elements, despite the fact that such ligands are currently used extensively in coordination chemistry. In view of the fact that a substituent in the 2-position exerts a direct influence on the steric environment of the metal center, we report here the application of the sterically demanding tris(1-tert-butyl-2-mercaptoimidazolyl)hydroborate [Tm^{{\rm Bu}^{\rm t}}] ligand to these metals. Dichlorido(η5-cyclopentadienyl)[tris(1-tert-butyl-2-sulfanylidene-2,3-dihydro-1H-imidazol-3-yl)borato-κ3S,S′,H]zirconium(IV) benzene hemisolvate, [Zr(C21H34BN6S3)(C5H5)Cl2]·0.5C6H6, (I), dichlorido(η5-cyclopentadienyl)[tris(1-tert-butyl-2-sulfanylidene-2,3-dihydro-1H-imidazol-3-yl)borato-κ3S,S′,H]titanium(IV) benzene hemisolvate, [Ti(C21H34BN6S3)(C5H5)Cl2]·0.5C6H6, (II), [bis(1-tert-butyl-2-sulfanylidene-2,3-dihydro-1H-imidazol-3-yl)borato-κ3S,S′,H]dichlorido(η5-cyclopentadienyl)zirconium(IV), [Zr(C14H24BN4S2)(C5H5)Cl2], (III), (1-tert-butyl-2,3-dihydro-1H-imidazole-2-thione-κS)(1-tert-butyl-2-sulfanylidene-1H-imidazol-3-ido-κ2N3,S)dichlorido(η5-cyclopentadienyl)zirconium(IV) benzene monosolvate, [Zr(C7H11N2S)(C7H12N2S)(C5H5)Cl2]·C6H6, (IV), and tribenzyl[tris(1-tert-butyl-2-sulfanylidene-2,3-dihydro-1H-imidazol-3-yl)borato-κ3S,S′,S′′]hafnium(IV) benzene tetrasolvate, [Hf(C7H7)3(C21H34BN6S3)]·4C6H6, (V), have been structurally characterized by X-ray diffraction. The [Tm^{{\rm Bu}^{\rm t}}^{{\rm Bu}^{\rm t}}] ligand coordinates to Ti and Zr in Cp[κ3S2,H-Tm^{{\rm Bu}^{\rm t}}]MCl2[M = Zr, (I), and Ti, (II)] in a κ3S2,Hmode, while the benzyl compounds [Tm^{{\rm Bu}^{\rm t}}]M(CH2Ph)3[M = Zr and Hf, (V)] exhibit κ3S3coordination.


2004 ◽  
Vol 23 (13) ◽  
pp. 3177-3183 ◽  
Author(s):  
Jarl Ivar van der Vlugt ◽  
Rafaël Sablong ◽  
Pieter C. M. M. Magusin ◽  
Allison M. Mills ◽  
Anthony L. Spek ◽  
...  

2020 ◽  
Author(s):  
Boris Sheludko ◽  
Cristina Castro ◽  
Chaitanya Khalap ◽  
Thomas Emge ◽  
Alan Goldman ◽  
...  

<b>Abstract:</b> The production of olefins via on-purpose dehydrogenation of alkanes allows for a more efficient, selective and lower cost alternative to processes such as steam cracking. Silica-supported pincer-iridium complexes of the form [(≡SiO-<sup>R4</sup>POCOP)Ir(CO)] (<sup>R4</sup>POCOP = κ<sup>3</sup>-C<sub>6</sub>H<sub>3</sub>-2,6-(OPR<sub>2</sub>)<sub>2</sub>) are effective for acceptorless alkane dehydrogenation, and have been shown stable up to 300 °C. However, while solution-phase analogues of such species have demonstrated high regioselectivity for terminal olefin production under transfer dehydrogenation conditions at or below 240 °C, in open systems at 300 °C, regioselectivity under acceptorless dehydrogenation conditions is consistently low. In this work, complexes <a>[(≡SiO-<i><sup>t</sup></i><sup>Bu4</sup>POCOP)Ir(CO)] </a>(<b>1</b>) and [(≡SiO-<i><sup>i</sup></i><sup>Pr4</sup>PCP)Ir(CO)] (<b>2</b>) were synthesized via immobilization of molecular precursors. These complexes were used for gas-phase butane transfer dehydrogenation using increasingly sterically demanding olefins, resulting in observed selectivities of up to 77%. The results indicate that the active site is conserved upon immobilization.


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