ChemInform Abstract: NMR AND IR STUDIES OF THE BONDING PROPERTIES OF THE ETHYLENE-RHODIUM COMPLEXES RHCL(C2H4)(L)(L′) (L = C2H4, CO, PR3, L′ = 2,6-LUTIDINE)

1978 ◽  
Vol 9 (47) ◽  
Author(s):  
A. MAISONNAT ◽  
R. POILBLANC
1994 ◽  
Vol 336 ◽  
Author(s):  
G. Lucovsky ◽  
M.J. Williams ◽  
S.S. He ◽  
S.M. Cho ◽  
Z. Jing ◽  
...  

ABSTRACTWe have incorporated N-atoms into hydrogenated amorphous silicon in the Si-rich alloy regime to ∼12 at.% N, and have observed a transition from n-type doping to alloying as the concentration of N-atoms is increased above about 5 at.%. By analogy with the local bonding arrangements of P-donors in n-doped a-Si:H, we attribute the doping to four-fold coordinated N-atoms with second neighbor H-atoms as in N+-Si-H linkages. The occurrence of these arrangements is supported by (i) IR studies which indicate a non-statistical association of N and H-atoms bonded to the same Si-atom, and (ii) a chemical bonding model in which the large effective electronegativies of four-fold coordinated N+ atoms and neutral O-atoms promote similar bonding properties with respect to their nearest-neighbor arrangements with Si and H atoms such as N+ (O) -Si-H linkages


2001 ◽  
Vol 79 (5-6) ◽  
pp. 578-586 ◽  
Author(s):  
Hanrong Gao ◽  
Robert J Angelici

Catalysts were prepared by adsorbing Rh2Cl2(CO)4 directly on gold powder or on gold that contained the tethered ligands 2-(diphenylphosphino)ethane-1-thiol (DPET) or methyl 2-mercaptonicotinate (MMNT). Infrared (IR) studies (diffuse reflectance infrared Fourier transform (DRIFT)) of the catalyst Rh–Au prepared by adsorbing Rh2Cl2(CO)4 directly on Au indicate that a RhI(CO)2 species is present. IR studies of Rh–DPET-Au suggest that tethered cis-Rh(DPET)(CO)2Cl is the major species at relatively high Rh2Cl2(CO)4 loadings, but trans-Rh(DPET)2(CO)Cl is observable at low Rh2Cl2(CO)4 loadings. Spectral investigations of the catalyst Rh–MMNT-Au prepared by adsorbing Rh2Cl2(CO)4 on MMNT-Au suggest that tethered [cis-Rh(MMNT)2(CO)2]+Cl– and (or) Rh(MMNT)(CO)2Cl are the major species at low Rh2Cl2(CO)4 loadings, while a new unidentified species predominates at high Rh2Cl2(CO)4 loadings. All three catalysts are active 1-hexene hydrogenation catalysts under the mild conditions of 40°C and 1 atm of H2; they are much more active than Au powder or Rh2Cl2(CO)4 in solution. Of the three catalysts, Rh–Au is the most active with a maximum turnover frequency (TOF) of 800 mol H2 per mol Rh per min while its turnover (TO) is 29 600 mol H2 per mol Rh during a 2-hour run. Under the conditions of 1-hexene hydrogenation, the catalysts lose their CO ligands. Thus, it appears that a form of Rh metal on Au is the catalytically active species.Key words: catalysis, olefin hydrogenation, gold powder, tethered rhodium complexes, infrared studies, adsorption, rhodium complexes.


1997 ◽  
Vol 07 (C1) ◽  
pp. C1-615-C1-616 ◽  
Author(s):  
I. Jacyna-Onyszkiewicz ◽  
M. Grunwald-Wyspianska ◽  
W. A. Kaczmarek

Author(s):  
D. Nagasamy Venkatesh ◽  
S. Karthick ◽  
M. Umesh ◽  
G. Vivek ◽  
R.M. Valliappan ◽  
...  

Roxythromycin/ β-cyclodextrin (Roxy/ β-CD) dispersions were prepared with a view to study the influence of β-CD on the solubility and dissolution rate of this poorly soluble drug. Phase-solubility profile indicated that the solubility of roxythromycin was significantly increased in the presence of β-cyclodextrin and was classified as AL-type, indicating the 1:1 stoichiometric inclusion complexes. Physical characterization of the prepared systems was carried out by differential scanning calorimetry (DSC), X-ray diffraction studies (XRD) and IR studies. Solid state characterization of the drug β-CD binary system using XRD, FTIR and DSC revealed distinct loss of drug crystallinity in the formulation, ostensibly accounting for enhancement of dissolution rate.


2006 ◽  
Vol 71 (2) ◽  
pp. 197-206 ◽  
Author(s):  
Martin Pošta ◽  
Jan Čermák ◽  
Pavel Vojtíšek ◽  
Ivana Císařová

The first rhodium complexes of diphosphinoazines [{RhCl(1,2-η:5,6-η-CH=CHCH2CH2CH=CHCH2CH2)}2 {μ-R2PCH2C(But)=NN=C(But)CH2PR2] (R = Ph, Cy, Pri) were prepared by cleavage of the bridge in chloro(cycloocta-1,5-diene)rhodium(I) dimer, the analogous iridium(I) complexes were also prepared for the first time. The X-ray structures of isostructural rhodium and iridium complexes with bis(dicyclohexylphosphino)pinacoloneazine were determined. Diphosphinoazine ligands in the complexes remained in (Z,Z) configuration bridging two RhCl(C8H12) units.


RSC Advances ◽  
2019 ◽  
Vol 9 (50) ◽  
pp. 29396-29404 ◽  
Author(s):  
Magdalena Jankowska-Wajda ◽  
Olga Bartlewicz ◽  
Andrea Szpecht ◽  
Adrian Zajac ◽  
Marcin Smiglak ◽  
...  

Platinum and rhodium complexes ligated by imidazolium substituted phosphine were obtained with high yields and applied as efficient catalysts.


Sign in / Sign up

Export Citation Format

Share Document