Zobrazeno 1 - 10
of 23
pro vyhledávání: '"James W. Raebiger"'
Autor:
H. N. Cheng, Richard A. Gross, Patrick B. Smith, Judit E. Puskas, Marcela Castano, Attila L. Gergely, Karla A. Barrera-Rivera, Ángel Marcos-Fernández, Antonio Martínez Richa, Florian Pion, Armando Félix Reano, Mouandhoime Zahahe Oulame, Imane Barbara, Amandine Léa Flourat, Paul-Henri Ducrot, Florent Allais, Andrew J. Maloney, Chenbo Dong, Alan S. Campbell, Cerasela Zoica Dinu, Jun-ichi Kadokawa, Gregory L. Côté, Christopher D. Skory, John Masani Nduko, Jian Sun, Seiichi Taguchi, Charles Romain, Charlotte K. Williams, J. P. MacDonald, M. P. Shaver, Seiichi Tada, Takanori Uzawa, Yoshihiro Ito, Nacú Hernández, Mengguo Yan, R. Christopher Williams, Eric Cochran, Kathleen O’Leary Havelka, Gregory E. Gerhardt, Jian Hong, Djavan Hairabedian, Zoran S Petrović, Andrew Myers, Atanu Biswas, Vijay Mannari, Chintankumar Patel, Wenyin Li, Ali Kiamanesh, Sanghoon Kim, Jonathan Jacoby, Marie-José Stébé, Nadia Canilho, Andreea Pasc, Giada Lo Re, Philippe Dubois, Jean-Marie Raquez, Silvia D. Luebben, James W. Raebiger, Kiyohiko Toyama, Makoto Soyama, Shukichi Ta
Publikováno v:
Carbon. 49:37-46
A simple method for extracting otherwise insoluble fullerenes into organic solvents is presented. The fullerenes are reduced to anionic charge states by contact with zinc in the presence of an alkylphosphonium salt in tetrahydrofuran. The anionic ful
Autor:
Timothy R. Filley, Caroline A. Masiello, James W. Raebiger, Brenda B. Bowen, Robert A. Blanchette, Robert D. Bolskar, Kathryn M. Schreiner, William C. Hockaday
Publikováno v:
Environmental Science & Technology. 43:3162-3168
Industrially produced carbon-based nanomaterials (CNM), including fullerenes and nanotubes, will be introduced into the environment in increasing amounts in the next decades. One likely environmental chemical transformation of C60 is oxidation to C60
Autor:
James W. Raebiger, Robert D. Bolskar
Publikováno v:
The Journal of Physical Chemistry C. 112:6605-6612
A comprehensive scheme for processing all arc-produced gadolinium monometallofullerenes into separate quantified fractions is presented. As generated by the carbon arc process, endohedral metallofullerenes are entrained in a complex mixture of more a
Autor:
Daniel L. DuBois, James W. Raebiger, Alex Miedaner, Jeffrey W. Turner, Calvin J. Curtis, Bruce C. Noll, Brian Cox
Publikováno v:
Organometallics. 25:3345-3351
The bis(triphosphine) ligand C6H4{P[CH2CH2P(C6H11)2]2}2, m-(triphos)2 (1), is synthesized by the reaction of m-bis(phosphino)benzene with 4 equiv of vinyldicyclohexylphosphine. Reaction of 1 with 2 equiv of [Pd(CH3CN)4](BF4)2 results in the formation
Autor:
Daniel L. DuBois, James W. Raebiger
Publikováno v:
Organometallics. 24:110-118
Four new rhodium complexes, [Rh(depx)2](CF3SO3), [(H)2Rh(depx)2](CF3SO3), [HRh(depx)2(CH3CN)](CF3SO3)2, and HRh(depx)2 (where depx = α,α‘-bis(diethylphosphino)xylene), have been synthesized and characterized. The pKa values of [(H)2Rh(depx)2]+ (3
Publikováno v:
Organometallics. 23:2670-2679
[HPt(EtXantphos)2](PF6) (where EtXantphos is 9,9-dimethyl-4,5-bis(diethylphosphino)xanthene) can be prepared by the reduction of Pt(COD)Cl2 (where COD is 1,4-cyclooctadiene) with hydrazine in the presence of 2 equiv of the diphosphine ligand followed
Autor:
Daniel L. DuBois, Susie M. Miller, Alex Miedaner, Calvin J. Curtis, Oren P. Anderson, James W. Raebiger
Publikováno v:
Journal of the American Chemical Society. 126:5502-5514
A series of [Pd(diphosphine)(2)](BF(4))(2) and Pd(diphosphine)(2) complexes have been prepared for which the natural bite angle of the diphosphine ligand varies from 78 degrees to 111 degrees. Structural studies have been completed for 7 of the 10 ne
Publikováno v:
Journal of the American Chemical Society. 126:2738-2743
The thermodynamic hydride donor abilities of 1-benzyl-1,4-dihydronicotinamide (BzNADH, 59 ± 2 kcal/mol), C5H5Mo(PMe3)(CO)2H (55 ± 3 kcal/mol), and C5Me5Mo(PMe3)(CO)2H (58 ± 2 kcal/mol) have been measured in acetonitrile by calorimetric and/or equi
Publikováno v:
Organometallics. 23:511-516
The complexes M(PNP)22+ (M = Pd, Pt, PNP = Et2PCH2N(Me)CH2PEt2) were synthesized by addition of PNP to Pd(CH3CN)4(BF4)2 and (COD)PtCl2, respectively. Pd(PNP)2 was synthesized by reaction of Pd(PNP)22+ with H2 and tetramethylguanidine (TMG) in CH3CN.