Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Travis J. Hebden"'
Publikováno v:
Organometallics. 36:3104-3109
A pair of POCOP-supported mono- and dicarbonyl complexes of Co have been prepared and crystallographically characterized. The reactivity of (tBuPOCOP)Co(CO) with H2, acids, and carbon monoxide has been compared to that of the previously reported Rh a
Autor:
Werner Kaminsky, Travis J. Hebden, D. Michael Heinekey, Dmitry G. Gusev, Karen I. Goldberg, Anthony J. St. John
Publikováno v:
Angewandte Chemie International Edition. 50:1873-1876
Ammonia borane (AB) is an attractive candidate for the chemical storage of hydrogen. Recently, our research group reported that the complex [(pocop)IrH2] (pocop= k -C6H31,3-[OP(tBu)2]2) has facilitated the rapid release of H2 from AB under mild condi
Autor:
Melanie C. Denney, D. Michael Heinekey, Vincent Pons, Karen I. Goldberg, Paula M. B. Piccoli, Arthur J. Schultz, Travis J. Hebden, Thomas F. Koetzle, Werner Kaminsky
Publikováno v:
Journal of the American Chemical Society. 130:10812-10820
Reaction of NaBH4 with (tBuPOCOP)IrHCl affords the previously reported complex (tBuPOCOP)IrH2(BH3) (1) (tBuPOCOP = kappa(3)-C6H3-1,3-[OP(tBu)2]2). The structure of 1 determined from neutron diffraction data contains a B-H sigma-bond to iridium with a
Autor:
Travis J. Hebden, D. Michael Heinekey, Karsten Krogh-Jespersen, Thomas J. Emge, Karen I. Goldberg, Xiawei Zhang, Alan S. Goldman
Publikováno v:
Inorganic chemistry. 49(4)
The iridium pincer complexes (PCP)IrH(4) (1; PCP = [kappa(3)-1,3-(CH(2)P(t)Bu(2))(2)C(6)H(3)]) and (POCOP)IrH(4) (2; POCOP = [kappa(3)-1,3-(OP(t)Bu(2))(2)C(6)H(3)]) have proven to be effective catalyst precursors for dehydrogenation of alkanes. The c
Publikováno v:
Journal of the American Chemical Society. 128(37)
In the presence of an iridium pincer complex, dehydrogenation of ammonia borane (H3NBH3) occurs rapidly at room temperature in tetrahydrofuran to generate 1.0 equivalent of H2 and [NH2BH2]5. A metal borohydride complex has been isolated as a dormant
Publikováno v:
Dalton transactions (Cambridge, England : 2003). (32)
A new ligand conceptually creates two sites reminiscent of beta-diketiminates, and upon deprotonation the salts exist in oligomeric forms with potassium ions linking multiple ligands.
Publikováno v:
Chemical Communications. 48:1851
(t-BuPOCOP)MoI(2) (1; t-BuPOCOP = C(6)H(3)-1,3-[OP(t-Bu)(2)](2)) has been synthesized from MoI(3)(THF)(3). Upon reduction of 1 with Na/Hg under dinitrogen molecular nitrogen is cleaved to form [(t-BuPOCOP)Mo(I)(N)](-). The origin of the N atom was co
Publikováno v:
Dalton Transactions: An International Journal of Inorganic Chemistry; Aug2006, Vol. 2006 Issue 32, p3855-3857, 3p