Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Todd W. Graham"'
Publikováno v:
Langmuir. 30:13301-13311
Oil-soluble phosphonium-based ionic liquids (ILs) have recently been reported as potential ashless lubricant additives. This study is to expand the IL chemistry envelope and to achieve fundamental correlations between the ion structures and ILs' phys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24f56dd1457631c3d53b19e16e3a55d2
https://doi.org/10.1021/la5032366
https://doi.org/10.1021/la5032366
Publikováno v:
Organometallics. 30:1382-1388
The first thermally stable, neutral, electrophilic phosphinidene complexes of vanadium, [CpV(CO)3{η1-P(NR2)}] (R = iPr (3a), Cy (3b)), have been prepared by the reaction of [Na]2[CpV(CO)3] with Cl2PNR2. The molecules 3a and 3b have been characterize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dbc53065aca4d0d48dfae7a516666f7
https://doi.org/10.1021/om100915v
https://doi.org/10.1021/om100915v
Autor:
Rongwei Guo, Shuiming Lu, Xuanhua Chen, Charles B. Ewart, Alan J. Lough, Christine Sui-Seng, Wenli Jia, Todd W. Graham, Chi-Wing Tsang, Dino Amoroso, Kamaluddin Abdur-Rashid
Publikováno v:
Angewandte Chemie International Edition. 49:8708-8711
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94d134273b0aab45d4b7287085b624a5
https://doi.org/10.1002/anie.201003074
https://doi.org/10.1002/anie.201003074
Publikováno v:
Organometallics. 27:3070-3081
The substituted diazoalkanes—ethyl diazoacetate (EDA), diethyl diazomalonate (DEDM), and trimethylsilyl diazomethane (TMSDM)—react readily with the methylene-bridged tricarbonyl species [RhM(CO)3(μ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffbd8253ebc7ab20a3e5bb38e484c1f9
https://doi.org/10.1021/om700756q
https://doi.org/10.1021/om700756q
Publikováno v:
Journal of Organometallic Chemistry. 692:4481-4485
The reaction of CpTi(μ 2 -Me)(μ 2 -NP i -Pr 3 )(μ 4 -C)(AlMe 2 ) 3 with ClSnMe 3 and MeO 3 SCF 3 affords the species CpTi(μ 2 -Cl)(μ 2 -NP i -Pr 3 )(μ 4 -C)(μ 2 -Cl)(AlMe)(AlMe 2 ) 2 1 and CpTi(μ 2 -Me)(μ 2 -NP i -Pr 3 )(μ 4 -C)(μ 2 -O 3 S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee040de97ce645a556796ff3f0b9b32e
https://doi.org/10.1016/j.jorganchem.2007.03.011
https://doi.org/10.1016/j.jorganchem.2007.03.011
Publikováno v:
Inorganica Chimica Acta. 360:1376-1379
The μ-phosphinidene complexes [Mn2(CO)8{μ-P(TMP)}] (1) (TMP = tetramethylpiperidyl) and [Mn2(CO)8{μ-P(NiPr2)}] (2) react with elemental sulfur to form rare phosphinidene sulfide complexes [Mn2(CO)9{μ-η1,η2-P(TMP) S}] (3) and [Mn2(CO)8{μ-η1,η
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b6ab3e417f1f2a9fd00e0536ef0531a
https://doi.org/10.1016/j.ica.2006.02.022
https://doi.org/10.1016/j.ica.2006.02.022
Autor:
Douglas W. Stephan, Christopher Fraser, Chunbao Zhu, Peter Voth, James W. Gauld, Todd W. Graham
Publikováno v:
Organometallics. 25:4779-4786
The reaction of the titanacycle CpTi(NPt-Bu3)(C4H8) (1) with benzyl halides, 4-bromo-1-butene, and allyl chloride proceeds with loss of ethylene to give CpTiX(NPt-Bu3)(CH2Ph) (X = Cl, 3; Br, 4), CpTiBr(NPt-Bu3)(CH2CH2CHCH2) (5), and CpTiCl(NPt-Bu3)(C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd5a9c112fe1895289e1de49f0cff374
https://doi.org/10.1021/om060565p
https://doi.org/10.1021/om060565p
Autor:
Michael J. Ferguson, Amala Chokshi, Martin R. Cowie, Robert McDonald, James R. Wigginton, Todd W. Graham
Publikováno v:
Organometallics. 24:6398-6410
Reaction of the methylene-bridged complex [RhOs(CO)3(μ-CH2)(dppm)2][CF3SO3] (dppm = μ-Ph2PCH2PPh2) with dimethyl acetylenedicarboxylate or hexafluorobutyne results in alkyne insertion into the Rh−CH2 bond, yielding [RhOs(CO)3(μ-η1:η1-RCC(R)CH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c499663f4fa510a6dd99c59006a89db
https://doi.org/10.1021/om058041x
https://doi.org/10.1021/om058041x
Publikováno v:
Organometallics. 23:3309-3318
The redox chemistry of phosphinimide-containing group IV metal complexes has been investigated. Reaction of the simple phosphinimide species CpTi(NPR3)Cl2 (R = Me 1, i-Pr 2) with Mg affords complexes formulated as [CpTiCl(μ-NPR3)]2 (R = Me 3, i-Pr 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::777266ad29cd7465fe7c3b6a11bad4dd
https://doi.org/10.1021/om049826q
https://doi.org/10.1021/om049826q
Publikováno v:
Scopus-Elsevier
The syntheses of a series of bifunctional ligands, in which a cyclopentadienyl and a phosphine group are linked by either a CH2 or a C2H4 fragment (-C5H4(CH2)nPR2; n = 1, 2; R = Me, Ph), are reported, as is that of the related ligand, Li2[Me2C(C5H3CM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d0aedb98156a1c0a876f662ff21837
https://doi.org/10.1021/om990279w
https://doi.org/10.1021/om990279w