نتایج جستجو برای: iridium nanoparticles

تعداد نتایج: 111183  

Journal: :The Journal of organic chemistry 2015
Scott A Sadler Andrew C Hones Bryan Roberts David Blakemore Todd B Marder Patrick G Steel

In the absence of a steric directing group, iridium-catalyzed C-H borylation of N-protected indazoles occurs rapidly and selectively at C-3 and the resulting boronate esters can be utilized in a range of downstream conversions. The functional group tolerance of the iridium-catalyzed C-H borylation reaction enables simple and efficient multidirectional syntheses of substituted indazoles to be re...

Journal: :Chemical communications 2015
Wei-Peng Liu Ming-Lei Yuan Xiao-Hui Yang Ke Li Jian-Hua Xie Qi-Lin Zhou

Highly efficient iridium catalyzed asymmetric transfer hydrogenation of simple ketones with ethanol as a hydrogen donor has been developed. By using chiral spiro iridium catalysts (S)- a series of alkyl aryl ketones were hydrogenated to chiral alcohols with up to 98% ee.

2015
Stafford W. Sheehan Julianne M. Thomsen Ulrich Hintermair Robert H. Crabtree Gary W. Brudvig Charles A. Schmuttenmaer

Molecular catalysts are known for their high activity and tunability, but their solubility and limited stability often restrict their use in practical applications. Here we describe how a molecular iridium catalyst for water oxidation directly and robustly binds to oxide surfaces without the need for any external stimulus or additional linking groups. On conductive electrode surfaces, this hete...

Journal: :Platinum Metals Review 2008

Journal: :Journal of the American Chemical Society 2007
Kevin C Fortner David S Laitar John Muldoon Lihung Pu Sonja B Braun-Sand Olaf Wiest Seth N Brown

Oxotrimesityliridium(V), (mes)3Ir=O (mes = 2,4,6-trimethylphenyl), and trimesityliridium(III), (mes)3Ir, undergo extremely rapid degenerate intermetal oxygen atom transfer at room temperature. At low temperatures, the two complexes conproportionate to form (mes)3Ir-O-Ir(mes)3, the 2,6-dimethylphenyl analogue of which has been characterized crystallographically. Variable-temperature NMR measurem...

Journal: :Pacing and clinical electrophysiology : PACE 2004
Kuan-Hung Yeh Chun-Chieh Wang Ming-Shien Wen Chung-Chuan Chou San-Jou Yeh Delon Wu

The long-term performance of two high impedance, steroid-eluting, passive-fixation ventricular leads, porous platinum iridium electrode CPI Selute Picotip 4035 (131 patients), and platinized platinum electrode Medtronic Capsure Z 5034 (57 patients), was compared with one conventional 8.0-mm2 porous platinum iridium electrode CPI Selute 4285 (38 patients). The mean follow-up period was 28 +/- 14...

Journal: :Chemical communications 2010
Hironobu Kanemitsu Ryosuke Harada Seiji Ogo

This work reports the synthesis and characterization of the first water-soluble iridium porphyrin, iridium(iii) diaqua porphyrin [Ir(III)(TSPP)(OH(2))(2)](3-) (1, TSPP = tetra-p-sulfonatophenyl porphyrin). The structure of 1 was unequivocally determined by single crystal X-ray analysis. Benzo-18-crown-6-ether is essential for producing single crystals suitable for X-ray analysis.

Journal: :Angewandte Chemie 2012
Chung-Hang Leung Hai-Jing Zhong Hui Yang Zhen Cheng Daniel Shiu-Hin Chan Victor Pui-Yan Ma Ruben Abagyan Chun-Yuen Wong Dik-Lung Ma

Staying in the pocket: A cyclometalated iridium(III) biquinoline complex targets the protein-protein interface (see picture; C yellow, N blue, Ir dark green) of the tumor necrosis factor-α (TNF-α) trimer. Molecular-modeling studies confirm the nature of this interaction. Both enantiomers of the iridium complex display comparable in vitro potency to the strongest small-molecule inhibitor of TNF-α.

2008
Heather A. Elsen Christopher F. Monson Marcin Majda

The properties of iridium oxide pH sensors produced by electrochemically induced deposition on gold electrodes were examined as a function of the composition of the deposition solution, as well as the electrochemical deposition protocol. The composition of the Ir IV deposition solutions, which included oxalate or ethylene diamine tetraacetic acid complexing agent or no complexing agent, had no ...

Journal: :Chemical communications 2014
H Schubert W Leis H A Mayer L Wesemann

A methylenediphenylphosphine substituted diazaborole was obtained in a two-step procedure in amounts around 4 g. This B-P ligand was coordinated at platinum and iridium and the structures of the boryl complexes are discussed. In the case of the iridium derivative an interesting boron-boron contact was found.

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