DSpace Repository

Transfer hydrogenation of ketones catalyzed by new rhodium and iridium

Show simple item record

dc.contributor.author Rafikova, K
dc.contributor.author Kystaubayeva, N
dc.contributor.author Aydemir, M
dc.contributor.author Kayan, C
dc.contributor.author Ocak, YS
dc.contributor.author Temel, H
dc.contributor.author Zazybin, A
dc.contributor.author Gurbuz, N
dc.contributor.author Ozdemir, I
dc.date.accessioned 2022-10-13T12:31:33Z
dc.date.available 2022-10-13T12:31:33Z
dc.date.issued 2014
dc.identifier.uri http://hdl.handle.net/11616/80001
dc.description.abstract The reaction of [Rh(mu-Cl)(cod)](2) and Ir(eta(5)-C5Me5)(mu-Cl)Cl](2) with aminophosphine ligands Cy2PNHCH2-C4H3X (X: O; S) gave a range of new monodendate [Rh(Cy(2)PNHCH(2)eC(4)H(3)O)(cod) Cl], (1), [Rh(Cy(2)PNHCH(2)eC(4)H3S)(cod) Cl], (2), [Ir(Cy2PNHCH2-C4H3O)(h(5)-C5Me5)Cl-2], (3) and [Ir(Cy2PNHCH2 -C4H3S)(eta(5)-C5Me5)Cl-2], (4) complexes, which were characterized by analytical and spectroscopic methods. The new rhodium(I) and iridium(III) catalysts were applied to transfer hydrogenation of acetophenone derivatives using 2-propanol as a hydrogen source. The results showed that the corresponding alcohols could be obtained with high activity (up to 99%) under mild conditions. Notably, [Rh(Cy2PNHCH2-C4H3O)(cod)Cl] complex (1) is much more active than the other analogous complexes in the transfer hydrogenation. Moreover, organiceinorganic rectifying contacts were fabricated forming rhodium(I) and iridium(III) complex thin films on n-Si semiconductors and evaporating Au metal on the structures. Electrical properties of the contacts including ideality factor, barrier height and series resistance were determined using their currentevoltage (IeV) data. The photoelectrical characteristics of the devices were examined under the light with 40-100 mW/cm(2) illumination conditions. It was seen that light had strong effects on IeV characteristics of the devices and the ones fabricated using 3 and 4 complexes had unusually forward and reverse bias photoconducting behavior. (C) 2014 Elsevier B.V. All rights reserved.
dc.description.abstract C1 [Rafikova, Khadichakhan; Kystaubayeva, Nurzhamal; Zazybin, Alexey] Kazakh British Tech Univ, Dept Chem Engn, Alma Ata 050000, Kazakhstan.
dc.description.abstract [Aydemir, Murat; Kayan, Cezmi] Dicle Univ, Dept Chem, Fac Sci, TR-21280 Diyarbakir, Turkey.
dc.description.abstract [Ocak, Yusuf Selim] Dicle Univ, Dept Sci, Fac Educ, TR-21280 Diyarbakir, Turkey.
dc.description.abstract [Temel, Hamdi] Dicle Univ, Dept Pharmaceut Chem, Fac Pharm, TR-21280 Diyarbakir, Turkey.
dc.description.abstract [Gurbuz, Nevin; Ozdemir, Ismail] Univ Inonu, Fac Sci & Art, Dept Chem, TR-44280 Malatya, Turkey.
dc.source JOURNAL OF ORGANOMETALLIC CHEMISTRY
dc.source LAR-CELLS; LIGANDS; SUZUKI; HYDROFORMYLATION; FABRICATION; HECK
dc.title Transfer hydrogenation of ketones catalyzed by new rhodium and iridium
dc.title complexes of aminophosphine containing cyclohexyl moiety and
dc.title photosensing behaviors of rhodium and iridium based devices


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record