@article {2168,
	title = {The complexes: RhCl(P-N)(THP), where P-N is P,N-chelated o-diphenylphosphino-N,N-dimethylaniline and THP is tris(hydroxymethyl)phosphine, and RhCl[(O)P-N][THP(O)] containing O-bonded phosphine oxides},
	journal = {Inorganica Chimica Acta},
	volume = {361},
	number = {11},
	year = {2008},
	note = {ISI Document Delivery No.: 323VATimes Cited: 3Cited Reference Count: 42Lorenzini, Fabio Patrick, Brian O. James, Brian R.},
	month = {Jul},
	pages = {3199-3204},
	type = {Article},
	abstract = {{The complex RhCl(P-N)(THP) (1) is synthesized under argon from RhCl(cod)(THP) and P-N, and is structurally characterized; P-N = P, N-chelated o-diphenylphosphino-N,N-dimethylaniline},
	keywords = {BEARING O-N, BIDENTATE PHOSPHINES, CATALYTIC-OXIDATION, HYDROFORMYLATION, LIGANDS, LOW-TEMPERATURE, N-DIMETHYLANILINYL SUBSTITUENTS, OXIDATION, PALLADIUM(II) COMPLEXES, phosphanes, phosphine oxides, phosphines, REACTIVITY, RHODIUM COMPLEXES, RHODIUM(I) COMPLEXES, X-ray structure},
	isbn = {0020-1693},
	url = {<Go to ISI>://000257475300029},
	author = {Lorenzini, F. and Patrick, B. O. and James, Brian R.}
}
@article {ISI:000251974000023,
	title = {An electronic rationale for observed initiation rates in ruthenium-mediated olefin metathesis: charge donation in phosphine and N-heterocyclic carbene ligands.},
	journal = {J. Am. Chem. Soc.},
	volume = {129},
	number = {51},
	year = {2007},
	month = {dec},
	pages = {15774{\textendash}6},
	chapter = {15774},
	abstract = {Ru K-edge XAS data indicate that second generation ruthenium-based olefin metathesis precatalysts (L = N-heterocyclic carbene) possess a more electron-deficient metal center than in the corresponding first generation species (L = tricyclohexylphosphine). This surprising effect is also observed from DFT calculations and provides a simple rationale for the slow phosphine dissociation kinetics previously noted for second-generation metathesis precatalysts.},
	keywords = {ALKENES, Alkenes: chemistry, BOND, carbenes, CATALYSTS, CL, DFT, ELECTRONS, Heterocyclic Compounds, Heterocyclic Compounds: chemistry, HYDROCARBONS, Hydrocarbons: chemistry, KINETICS, LIGANDS, MECHANISM, METHANE, Methane: analogs \& derivatives, Methane: chemistry, MOIETY, NHC LIGANDS, OLEFIN METATHESIS, phosphines, Phosphines: chemistry, RAY-ABSORPTION SPECTROSCOPY, ruthenium, Ruthenium: chemistry, TRANSITION-METAL-COMPLEXES, XAS},
	isbn = {0002-7863},
	issn = {1520-5126},
	doi = {10.1021/ja0747674},
	url = {<Go to ISI>://000251974000023 http://www.ncbi.nlm.nih.gov/pubmed/18047332},
	author = {Getty, Kendra and Delgado-Jaime, Mario Ulises and Kennepohl, Pierre}
}
@article {1499,
	title = {New oligophosphines and (hydroxymethyl)phosphonium chlorides},
	journal = {Inorganic Chemistry},
	volume = {45},
	number = {7},
	year = {2006},
	note = {ISI Document Delivery No.: 028HCTimes Cited: 6Cited Reference Count: 46},
	month = {Apr},
	pages = {2917-2924},
	type = {Article},
	abstract = {{The new oligophosphines [H2P(CH2)(2)](2)PH, [H2P(CH2)(2)P(H)CH2](2), and {[(H2P(CH2)(2)](2)PCH2}(2) have been made by hydrophosphination of diethyl vinylphosphonate (2) with H2P(CH2)(2)PH2 (1), using different ratios of 2/1, followed by LiAlH4 reduction of the phosphonate intermediates; the three phosphonate precursors were obtained as oils of varying purity (similar to 90-95\%) in low (similar to 20\%) to almost quantitative yield. The tri-, tetra-, and hexaphosphines were then treated with formaldehyde in the presence of hydrochloric acid to generate the corresponding water-soluble (hydroxymethyl)phosphonium chlorides {(HOCH2)(3)P[(CH2)(2)P(CH2OH)(2)](n)(CH2)(2)P(CH2PH)(3)}Cl-m (n = 1},
	keywords = {ALDEHYDES, BRIGHTNESS STABILIZING AGENTS, COMPLEXES, CRYSTAL-STRUCTURE, DERIVATIVES, FORMALDEHYDE, LIGANDS, phosphines, SALTS, WATER},
	isbn = {0020-1669},
	url = {<Go to ISI>://000236476700018},
	author = {Moiseev, D. and James, Brian R. and Patrick, B. O. and Hu, Thomas Q.}
}
@article {1499,
	title = {New oligophosphines and (hydroxymethyl)phosphonium chlorides},
	journal = {Inorganic Chemistry},
	volume = {45},
	number = {7},
	year = {2006},
	note = {ISI Document Delivery No.: 028HCTimes Cited: 6Cited Reference Count: 46},
	month = {Apr},
	pages = {2917-2924},
	type = {Article},
	abstract = {{The new oligophosphines [H2P(CH2)(2)](2)PH, [H2P(CH2)(2)P(H)CH2](2), and {[(H2P(CH2)(2)](2)PCH2}(2) have been made by hydrophosphination of diethyl vinylphosphonate (2) with H2P(CH2)(2)PH2 (1), using different ratios of 2/1, followed by LiAlH4 reduction of the phosphonate intermediates; the three phosphonate precursors were obtained as oils of varying purity (similar to 90-95\%) in low (similar to 20\%) to almost quantitative yield. The tri-, tetra-, and hexaphosphines were then treated with formaldehyde in the presence of hydrochloric acid to generate the corresponding water-soluble (hydroxymethyl)phosphonium chlorides {(HOCH2)(3)P[(CH2)(2)P(CH2OH)(2)](n)(CH2)(2)P(CH2PH)(3)}Cl-m (n = 1},
	keywords = {ALDEHYDES, BRIGHTNESS STABILIZING AGENTS, COMPLEXES, CRYSTAL-STRUCTURE, DERIVATIVES, FORMALDEHYDE, LIGANDS, phosphines, SALTS, WATER},
	isbn = {0020-1669},
	url = {<Go to ISI>://000236476700018},
	author = {Moiseev, D. and James, Brian R. and Patrick, B. O. and Hu, Thomas Q.}
}
@article {1137,
	title = {A new class of bleaching and brightness stabilizing agents. Part II: Bleaching power of a bisphosphine},
	journal = {Journal of Pulp and Paper Science},
	volume = {31},
	number = {2},
	year = {2005},
	note = {ISI Document Delivery No.: 940RYTimes Cited: 11Cited Reference Count: 35},
	month = {Apr-Jun},
	pages = {69-75},
	type = {Article},
	abstract = {Recently we discovered that simple, water-soluble phosphorus compounds such as tris(hydroxymethyl)phosphine, P(CH2OH)(3) (THP), were effective bleaching agents for mechanical pulps over a wide range of consistency, pH and temperature. Now, we have found a bisphoslethine derivative of THP, 1,2-bis[bis(hydroxymethyl)phosphino]ethane, (HOCH2)(2)PCH2CH2P(CH2OH)(2)(BBHPE),to be even more effective than THP. This derivative pable of providing an ISO brightness gain of 13.0 and 15.2 points to spruce and pine thermomechanical pulps (TMP), respectively, compared to a maximum ISO brightness gain of similar to 10.0 points achievable with THP or sodium hydrosulphite. BBHPE is particularly useful as a bleaching agent for pulps that have a poor bleach response to sodium hydrosulphite. It also shows promise as a complementary bleaching agent to alkaline hydrogen peroxide. The bisphosphonium sulphate [(HOCH2)(3)pCH(2)CH(2)P(CH2OH)(3)]SO4 has also been synthesized and shown to be nearly as effective as BBHPE for the bleaching of spruce TMP and peroxide-bleached spruce TMP.},
	keywords = {bleach, brightness, mechanical pulps, phosphines, phosphorus compounds, picea, pinus, SOLUBILITY},
	isbn = {0826-6220},
	url = {<Go to ISI>://000230163000001},
	author = {Hu, Thomas Q. and James, Brian R. and Yawalata, D. and Ezhova, M. B. and Chandra, R. P.}
}
@article {1137,
	title = {A new class of bleaching and brightness stabilizing agents. Part II: Bleaching power of a bisphosphine},
	journal = {Journal of Pulp and Paper Science},
	volume = {31},
	number = {2},
	year = {2005},
	note = {ISI Document Delivery No.: 940RYTimes Cited: 11Cited Reference Count: 35},
	month = {Apr-Jun},
	pages = {69-75},
	type = {Article},
	abstract = {Recently we discovered that simple, water-soluble phosphorus compounds such as tris(hydroxymethyl)phosphine, P(CH2OH)(3) (THP), were effective bleaching agents for mechanical pulps over a wide range of consistency, pH and temperature. Now, we have found a bisphoslethine derivative of THP, 1,2-bis[bis(hydroxymethyl)phosphino]ethane, (HOCH2)(2)PCH2CH2P(CH2OH)(2)(BBHPE),to be even more effective than THP. This derivative pable of providing an ISO brightness gain of 13.0 and 15.2 points to spruce and pine thermomechanical pulps (TMP), respectively, compared to a maximum ISO brightness gain of similar to 10.0 points achievable with THP or sodium hydrosulphite. BBHPE is particularly useful as a bleaching agent for pulps that have a poor bleach response to sodium hydrosulphite. It also shows promise as a complementary bleaching agent to alkaline hydrogen peroxide. The bisphosphonium sulphate [(HOCH2)(3)pCH(2)CH(2)P(CH2OH)(3)]SO4 has also been synthesized and shown to be nearly as effective as BBHPE for the bleaching of spruce TMP and peroxide-bleached spruce TMP.},
	keywords = {bleach, brightness, mechanical pulps, phosphines, phosphorus compounds, picea, pinus, SOLUBILITY},
	isbn = {0826-6220},
	url = {<Go to ISI>://000230163000001},
	author = {Hu, Thomas Q. and James, Brian R. and Yawalata, D. and Ezhova, M. B. and Chandra, R. P.}
}
@article {887,
	title = {A new class of bleaching and brightness stabilizing agents. Part I: Bleaching of mechanical Pulps},
	journal = {Journal of Pulp and Paper Science},
	volume = {30},
	number = {8},
	year = {2004},
	note = {ISI Document Delivery No.: 860FETimes Cited: 14Cited Reference Count: 43},
	month = {Aug},
	pages = {233-240},
	type = {Article},
	abstract = {We have discovered a new class of bleaching and brightness stabilizing agents for mechanical and chemical pulps. The new agents are water-soluble tertiary phosphines and quaternary hydroxymethyl phosphonium salts, such as tris(hydroxymethyl)phosphine (THP), P(CH2OH)(3), and tetrakis(hydroxymethyl)phosphonium chloride (THPC), [P(CH2OH)(4)]Cl. For the bleaching of mechanical pulps, such phosphorus compounds have a bleaching power similar to that of sodium hydrosulphite, but they can be used over a wider range of pH (4.3-9.3), temperature (20-130degreesC) and consistency(e.g. 1.5-20\%) without the need for the removal of oxygen or transition metal ions. Furthermore, pulps bleached with this new class of bleaching agents show higher heat and moisture stability than those bleached with sodium hydrosulphite or alkaline hydrogen peroxide. Bleaching of mechanical pulps with THP or THPC is accompanied by a reduction of the absorption coefficient of the pulps.},
	keywords = {bleach, bleaching, DISULFIDES, evaluation, mechanical pulps, PERFORMANCE, phosphines, phosphonium compounds, pulp properties, REDUCTION, stabilizers, tertiary compounds},
	isbn = {0826-6220},
	url = {<Go to ISI>://000224327100005},
	author = {Hu, Thomas Q. and James, Brian R. and Yawalata, D. and Ezhova, M. B.}
}
@article {887,
	title = {A new class of bleaching and brightness stabilizing agents. Part I: Bleaching of mechanical Pulps},
	journal = {Journal of Pulp and Paper Science},
	volume = {30},
	number = {8},
	year = {2004},
	note = {ISI Document Delivery No.: 860FETimes Cited: 14Cited Reference Count: 43},
	month = {Aug},
	pages = {233-240},
	type = {Article},
	abstract = {We have discovered a new class of bleaching and brightness stabilizing agents for mechanical and chemical pulps. The new agents are water-soluble tertiary phosphines and quaternary hydroxymethyl phosphonium salts, such as tris(hydroxymethyl)phosphine (THP), P(CH2OH)(3), and tetrakis(hydroxymethyl)phosphonium chloride (THPC), [P(CH2OH)(4)]Cl. For the bleaching of mechanical pulps, such phosphorus compounds have a bleaching power similar to that of sodium hydrosulphite, but they can be used over a wider range of pH (4.3-9.3), temperature (20-130degreesC) and consistency(e.g. 1.5-20\%) without the need for the removal of oxygen or transition metal ions. Furthermore, pulps bleached with this new class of bleaching agents show higher heat and moisture stability than those bleached with sodium hydrosulphite or alkaline hydrogen peroxide. Bleaching of mechanical pulps with THP or THPC is accompanied by a reduction of the absorption coefficient of the pulps.},
	keywords = {bleach, bleaching, DISULFIDES, evaluation, mechanical pulps, PERFORMANCE, phosphines, phosphonium compounds, pulp properties, REDUCTION, stabilizers, tertiary compounds},
	isbn = {0826-6220},
	url = {<Go to ISI>://000224327100005},
	author = {Hu, Thomas Q. and James, Brian R. and Yawalata, D. and Ezhova, M. B.}
}
@article {716,
	title = {Dichloro(diphosphine)(2-pyridyl-ketone)ruthenium(II) complexes},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {81},
	number = {11},
	year = {2003},
	note = {ISI Document Delivery No.: 746YXTimes Cited: 9Cited Reference Count: 31},
	month = {Nov},
	pages = {1263-1269},
	type = {Article},
	abstract = {Described are the synthesis and characterization of Ru(II) complexes of the type RuCl2L2(N-O), where L-2 is either 1,4-bis(diphenylphosphino)butane (dppb) or (PPh3)(2), and N-O represents chelated 2-benzoylpyridine (2-bzpy) or 2-acetylpyridine (2-acpy); the Ru presursors used were [RuCl2(dppb)](2)(mu-dppb) or RuCl2(PPh3)(3). The crystal structure of cis-RuCl2(dppb)(2-bzpy) is presented, and three other RuCl2L2(N-O) complexes with cis-chlorines are isolated and characterized spectroscopically; of the trans-dichloro species, RuCl2(PPh3)(2)(N-O) complexes are isolated, while the corresponding dppb species are characterized in situ. In all cases, thermodynamically stable cis-complexes are formed from initially formed trans-species.},
	keywords = {2, 2-acetylpyridine, 2-benzoylpyridine, 2{\textquoteright}-BIPYRIDINE, CRYSTAL-STRUCTURE, DONOR, ISOMERIZATION, LIGANDS, phosphines, REDOX POTENTIALS, ruthenium, ruthenium complexes, structures, X-RAY},
	isbn = {0008-4042},
	url = {<Go to ISI>://000186777600018},
	author = {Queiroz, S. L. and Batista, A. A. and de Araujo, M. P. and Bianchini, R. C. and Oliva, G. and Ellena, J. and James, Brian R.}
}
@article {609,
	title = {Interaction of rhodium(I) bisphosphine complexes with semicarbazones to give orthometallated rhodium(III) complexes},
	journal = {Russian Chemical Bulletin},
	volume = {52},
	number = {12},
	year = {2003},
	note = {ISI Document Delivery No.: 809IUTimes Cited: 7Cited Reference Count: 57International Memorial Symposium on Modern Trends in Organometallic and Catalytic Chemistry Dedicated to Mark Vol{\textquoteright}pinMAY 18-AUG 23, 2003Moscow, RUSSIA},
	month = {Dec},
	pages = {2707-2714},
	type = {Proceedings Paper},
	abstract = {Interaction of the cis-[Rh(PR3)(2)(Solv)(2)]PF6 complexes (R = Ar or R-3 = Ph2Me, Solv solvent) under Ar with semicarbazones bearing a phenyl group on the imine-C atom gives the rhodium(III)-hydrido-bis(phosphine)-orthometallated semicarbazone species [RhH(PR3)(2){(o-C6H4(R{\textquoteright})C=N-N(H)CONH2}]PF6 (R{\textquoteright} = Me or Et), which are characterized generally by elemental analysis, P-31{H-1} and H-1 NMR spectroscopy, and mass-spectrometry. The PPh3-containing complex with R{\textquoteright} = Me, structurally characterized by X-ray analysis, reveals coordination of the semicarbazone by the ortho-C atom, the imine-N atom, and the amide-carbonyl group. For a semicarbazone containing no Ph group, the rhodium(I) complex [Rh(PR3)(2)(Et(Me)C=N-N(H)CONH2)]PF6, containing the eta(2)-semicarbazone bonded via the imine-N and carbonyl, is formed. Attempts to hydrogenate the C=N moiety in the complexes or to catalytically hydrogenate the semicarbazones were unsuccessful.},
	keywords = {ACTIVATION, ASYMMETRIC HYDROGENATION, BENZALDEHYDE SEMICARBAZONE, C-H, C-H BONDS, CATALYTIC-HYDROGENATION, COMPLEXES, CRYSTAL-STRUCTURE, FINE CHEMICALS, INTRAMOLECULAR ACTIVATION, molecular structure, orthometallation, phosphines, rhodium, SELECTIVE HYDROGENATION, semicarbazones, SYNTHESIS, TRANSITION-METAL-COMPLEXES, UNPRECEDENTED CHEMICAL TRANSFORMATION},
	isbn = {1066-5285},
	url = {<Go to ISI>://000220631200019},
	author = {Ezhova, M. B. and Patrick, B. O. and James, Brian R. and Ford, M. E. and Waller, E. J.}
}
@article {3005,
	title = {CHARACTERIZATION AND NONRIGID BEHAVIOR OF A CARBOXYLATE-BRIDGED RHODIUM DIMER},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {72},
	number = {5},
	year = {1994},
	note = {ISI Document Delivery No.: NU280Times Cited: 0Cited Reference Count: 47},
	month = {May},
	pages = {1294-1301},
	type = {Article},
	abstract = {{Bis(mu-t-butylacetato)bis(norbornadiene)dirhodium(I) 1 is prepared by a reaction between pivaloyl camphor and (norbornadiene)rhodium(I) chloride dimer. A molecular rearrangement takes place in which the pivaloyl groups of the pivaloyl camphor starting material are incorporated into the end product as bridging t-butylcarboxylate ligands. A variable temperature H-1 NMR study and corresponding dynamic computer fit of the NMR data, and crystal structure are reported for the structurally nonrigid dimer. Crystals of 1 are triclinic},
	keywords = {BINUCLEAR DIRHODIUM COMPOUNDS, CATALYSTS, COMPLEXES, CRYSTAL, ELECTRONIC-STRUCTURE, LIGANDS, MOLECULAR-STRUCTURE, ORTHO-METALATION REACTIONS, phosphines, RH-RH BOND},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1994NU28000012},
	author = {Cullen, W. R. and Rettig, S. J. and Wickenheiser, E. B.}
}
@article {3216,
	title = {MULTINUCLEAR COMPLEXES DERIVED FROM FERROCENYLPHOSPHINES AND TRIRUTHENIUM DODECACARBONYL},
	journal = {Organometallics},
	volume = {13},
	number = {9},
	year = {1994},
	note = {ISI Document Delivery No.: PF967Times Cited: 11Cited Reference Count: 37},
	month = {Sep},
	pages = {3594-3604},
	type = {Article},
	abstract = {{Pyrolysis of Ru-3(CO)(1)1(PFc(2)Ph) in hexanes for 15 h gave the trinuclear cluster Ru-3(CO)(8)(mu CO)(mu-H)[mu-eta(3)-(eta(5)-C(5)H(3)PFcPh)Fe(eta(5)-C5H5)] (11) in 20\% yield. Pyrolysis of Ru-3(CO)(12) with PFc(2)Ph in octane for 3.5 h gave the tetranuclear cluster RU(4)(CO)(11)(mu(3)-PFc)(mu-eta(1):eta(5)-C5H4) (12) in 12\% yield and the previously known 8, RU(4)(CO)(10)(mu-CO)mu(4)-PFc)(mu(4)-C6H4), in 10 yield: the mild conditions are noteworthy. Pyrolysis of Ru-3(CO)(12) With PEt(2)Fc in octane for 18 h gave the hexanuclear cluster complexes RU(6)C(CO)(14)(mu-PEt(2))(2) (13) and RU(6)C(CO)(13)(mu-PEt(2))(eta(5)-C5H5) (14) in 15\% and 25\% yields, respectively, and the pentanuclear derivative Ru-5(CO)(9)(mu-CO)(eta(6)-C6H6)(2)(mu(4)-PEt) (15) (low yield). Pyrolysis Of Ru-3(CO)(12) with PEtFc(2) in toluene for 10 h gave the pentanuclear cluster RU(5)(CO)(12)(mu(4)-PEt)(eta(6)-C7H8) (16) in similar to 5\% yield. Crystal data: 8, monoclinic, space group P2(1)/c},
	keywords = {benzene, MODE, MOLECULAR-STRUCTURES, OSMIUM CLUSTER, PH, phosphines, RAY CRYSTAL-STRUCTURE, RU3(CO)12, ruthenium, THERMOLYSIS},
	isbn = {0276-7333},
	url = {<Go to ISI>://A1994PF96700036},
	author = {Zheng, T. C. and Cullen, W. R. and Rettig, S. J.}
}
