@article {ANIE:ANIE201511448,
	title = {Capturing HBCy2: Using N,O-Chelated Complexes of Rhodium(I) and Iridium(I) for Chemoselective Hydroboration},
	journal = {Angewandte Chemie International Edition},
	volume = {55},
	number = {9},
	year = {2016},
	pages = {3181{\textendash}3186},
	keywords = {boranes, hemilability, hydroboration, IRIDIUM, rhodium},
	issn = {1521-3773},
	doi = {10.1002/anie.201511448},
	url = {http://dx.doi.org/10.1002/anie.201511448},
	author = {Drover, Marcus W. and Schafer, Laurel L. and Love, Jennifer A.}
}
@article {ANIE:ANIE201511448,
	title = {Capturing HBCy2: Using N,O-Chelated Complexes of Rhodium(I) and Iridium(I) for Chemoselective Hydroboration},
	journal = {Angewandte Chemie International Edition},
	volume = {55},
	number = {9},
	year = {2016},
	pages = {3181{\textendash}3186},
	abstract = {1,3-N,O-chelated complexes of RhI and IrI cooperatively and reversibly stabilized the B-H bond of HBCy2 to afford six-membered metallaheterocycles (M=Rh (7) or Ir (8)) having a δ-[M]...H-B agostic interaction. Treatment of these Shimoi-type borane adducts 7 or 8 with both an aldehyde and an alkene resulted in chemoselective aldehyde hydroboration and reformation of the 1,3-N,O-chelated starting material. The observed chemoselectivity is inverted from that of free HBCy2, which is selective for alkene hydroboration.},
	keywords = {boranes, hemilability, hydroboration, IRIDIUM, rhodium},
	issn = {1521-3773},
	doi = {10.1002/anie.201511448},
	url = {http://dx.doi.org/10.1002/anie.201511448},
	author = {Drover, Marcus W. and Schafer, Laurel L. and Love, Jennifer A.}
}
@article {CHEM:CHEM201600951,
	title = {Phosphoramidate-Supported Cp*IrIII Aminoborane H2B=NR2 Complexes: Synthesis, Structure, and Solution Dynamics},
	journal = {Chemistry {\textendash} A European Journal},
	volume = {22},
	number = {20},
	year = {2016},
	pages = {6793{\textendash}6797},
	keywords = {aminoboranes, B-H activation, density functional calculations, IRIDIUM, ligand effects},
	issn = {1521-3765},
	doi = {10.1002/chem.201600951},
	url = {http://dx.doi.org/10.1002/chem.201600951},
	author = {Drover, Marcus W. and Bowes, Eric G. and Schafer, Laurel L. and Love, Jennifer A. and Weller, Andrew S.}
}
@article {CHEM:CHEM201600951,
	title = {Phosphoramidate-Supported Cp*IrIII Aminoborane H2B=NR2 Complexes: Synthesis, Structure, and Solution Dynamics},
	journal = {Chemistry {\textendash} A European Journal},
	volume = {22},
	number = {20},
	year = {2016},
	pages = {6793{\textendash}6797},
	abstract = {Reaction of aminoboranes H2B=NR2 (R=iPr or Cy) with the cationic Cp*IrIII phosphoramidate complex [IrCp*{κ2-N,O-Xyl(N)P(O)(OEt)2}][BArF4] generates the aminoborane complexes [IrCp*(H){κ1-N-η2-HB-Xyl(N)P(OBHNR2)(OEt)2}][BArF4] (R=iPr or Cy) in which coordination of a P=O bond with boron weakens the B=N multiple bond. For these complexes, solution- and solid-state, as well as DFT computational techniques, have been employed to substantiate B-N bond rotation of the coordinated aminoborane.},
	keywords = {aminoboranes, B-H activation, density functional calculations, IRIDIUM, ligand effects},
	issn = {1521-3765},
	doi = {10.1002/chem.201600951},
	url = {http://dx.doi.org/10.1002/chem.201600951},
	author = {Drover, Marcus W. and Bowes, Eric G. and Schafer, Laurel L. and Love, Jennifer A. and Weller, Andrew S.}
}
@article {2116,
	title = {Amine-tethered N-heterocyclic carbene complexes of rhodium(I)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {86},
	number = {8},
	year = {2008},
	note = {ISI Document Delivery No.: 329TMTimes Cited: 9Cited Reference Count: 50Jong, Howard Patrick, Brian O. Fryzuk, Michael D.},
	month = {Aug},
	pages = {803-810},
	type = {Article},
	abstract = {A new family of rhodium-diene based complexes has been developed that incorporates an N-heterocyclic carbene ligand with an N-donor tether. The ligand is denoted (Mes)[CNH] 2 (where (Mes)[CNH] is 2,4,6-Me3C6H2NC3H2NCH2CH2NH-2,4,6-Me3C6H2) and (Mes)[CN] for the amido form. The synthesis of the (Mes)[CNH] ligand involves reaction of N-mesitylimidazole with 2-chloroethyl-N-mesitylamine under melt conditions, followed by deprotonation with KN(SiMe3)(2). The reaction of (Mes)[CNH] with [(diene)RhCl](2) results in the formation of the monodentate complexes, (Mes)[CNH]Rh(diene)Cl (where diene = 1,5-cyclooctadiene (COD): 3a; diene = 2,5-norbornadiene (NBD): 3b). Bidentate variants could be isolated as either a neutral species, (Mes)[CN]Rh(diene) 4a-4b, via deprotonation, or an ionic analogue such as [(Mes)[CNH]Rh(diene)]BF4 5a-5b by reaction with NaBF4. Compounds 4-5 are the first examples of rhodium compounds that contained a bidentate NHC ligand with a pendant amino or amido donor. Complexes 3-5 were characterized fully and the solid-state single crystal X-ray structures of 3a, 4a, and 5b are discussed. The utility of these complexes as catalyst precursors for hydrogenation reactions was examined and it was determined that these systems are not significantly more active than colloidal rhodium when parallel reactions were run. Various methods of transfer hydrogenations were also investigated with 3a, which did not yield an appreciable conversion of either benzophenone or N-benzylideneaniline as substrates.},
	keywords = {CATALYSIS, HYDROGENATION, HYDROSILYLATION CATALYSTS, imines, IRIDIUM, KETONES, LIGANDS, N-heterocyclic carbene, REACTIVITY, rhodium, SEARCH, STABLE CARBENES, TRANSFER HYDROGENATION},
	isbn = {0008-4042},
	url = {<Go to ISI>://000257893500010},
	author = {Jong, H. and Patrick, B. O. and Fryzuk,Michael D.}
}
@article {2063,
	title = {Chiral Ligand Design: A Bidentate Ligand Incorporating an Acyclic Phosphaalkene},
	journal = {Angewandte Chemie-International Edition},
	volume = {47},
	number = {42},
	year = {2008},
	note = {ISI Document Delivery No.: 360YLTimes Cited: 7Cited Reference Count: 71Dugal-Tessier, Julien Dake, Gregory R. Gates, Derek P.},
	pages = {8064-8067},
	type = {Article},
	keywords = {ALKYLATION, ALLYLIC, BEARING DIPHOSPHINIDENECYCLOBUTENE LIGANDS, BIPHOSPHININE COMPLEXES, CATALYZED ASYMMETRIC, CLAISEN REARRANGEMENT, COORDINATION PROPERTIES, ENANTIOSELECTIVE ISOMERIZATION, ETHYLENE POLYMERIZATION, HIGHLY-ACTIVE CATALYSTS, HYDROGENATION, IRIDIUM, ligand design, N, P-ligands, PHOSPHAALKENES, PHOSPHORUS, PI-ACCEPTOR LIGANDS},
	isbn = {1433-7851},
	url = {<Go to ISI>://000260094600016},
	author = {Dugal-Tessier, J. and Dake, G. R. and Gates, D. P.}
}
@article {1646,
	title = {New rhodium(I) carbene complexes from carbene transfer reactions},
	journal = {Organometallics},
	volume = {25},
	number = {9},
	year = {2006},
	note = {ISI Document Delivery No.: 035AZTimes Cited: 25Cited Reference Count: 41},
	month = {Apr},
	pages = {2359-2363},
	type = {Article},
	abstract = {The Rh(I) complexes RhCl(diene)(NHC) have been synthesized from Ag(I) carbene precursors, where NHC is one of the N-heterocyclic carbenes 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (IPr), 1,3bis(2,4,6-trimethylphenyl)imidazol-2-ylidene (IMes), 3-methyl-1-phenacylimidazol-2-ylidene (MAI), and 3-methyl-1-picolylimidazol-2-ylidene (MPI), and diene is either NBD or COD. The complexes are characterized by elemental analysis, H-1 NMR and IR spectroscopies, mass spectrometry, and, in the case of RhCl(NBD)(IMes) and RhCl(COD)(MAI), X-ray crystallography. The new Ag(I) carbene complexes [Ag(IPr)(2)]PF6 and [Ag(IMeS)(2)]PF6 are also reported.},
	keywords = {APPLICATION, CATALYTIC, COUPLING, EFFICIENT CATALYSTS, IRIDIUM, LIGAND, METAL-COMPLEXES, N-heterocyclic carbene, NUCLEOPHILIC CARBENE, OLEFIN METATHESIS, REACTIONS, SILVER(I)},
	isbn = {0276-7333},
	url = {<Go to ISI>://000236973500033},
	author = {Yu, X. Y. and Patrick, B. O. and James, Brian R.}
}
@article {1605,
	title = {Ortho-selective C-Hactivation of substituted benzenes effected by a tungsten alkylidene complex without substituent coordination},
	journal = {Organometallics},
	volume = {25},
	number = {17},
	year = {2006},
	note = {ISI Document Delivery No.: 070PZTimes Cited: 13Cited Reference Count: 36Tsang, Jenkins Y. K. Buschhaus, Miriam S. A. Legzdins, Peter Patrick, Brian O.},
	month = {Aug},
	pages = {4215-4225},
	type = {Article},
	abstract = {{Gentle thermolysis of the bis(neopentyl) complex Cp*W(NO)(CH2CMe3)(2) (1) at 70 degrees C in various substituted benzenes results in the loss of neopentane and the generation of the transient alkylidene complex Cp*W(NO)(=CHCMe3) (A), which subsequently effects single C-H bond activations of the benzenes. These activations exhibit a pronounced selectivity for the C-H linkages ortho to the benzene substituents. Thus, thermal reactions of 1 with C6H5X lead to the preferential formation of the corresponding Cp*W( NO)(CH2CMe3)(o-C6H4X) complexes, the ortho-selectivity, i. e.},
	keywords = {CLEAVAGE, CRYSTAL-STRUCTURE, ELIMINATION, H BONDS, IRIDIUM, MECHANISM, METAL-COMPLEXES, {ARYL},
	isbn = {0276-7333},
	url = {<Go to ISI>://000239536800028},
	author = {Tsang, J. Y. K. and Buschhaus, M. S. A. and Legzdins,Peter and Patrick, B. O.}
}
@article {7018,
	title = {SYNTHESIS AND REACTIVITY OF RUTHENIUM AMIDE PHOSPHINE COMPLEXES - FACILE CONVERSION OF A RUTHENIUM AMIDE TO A RUTHENIUM AMINE VIA DIHYDROGEN ACTIVATION AND ORTHO METALATION - X-RAY STRUCTURE OF RUCL(C6H4PPH2)[NH(SIME2CH2PPH2)2]},
	journal = {Organometallics},
	volume = {10},
	number = {2},
	year = {1991},
	note = {ISI Document Delivery No.: EY681Times Cited: 68Cited Reference Count: 38},
	month = {Feb},
	pages = {467-473},
	type = {Article},
	abstract = {{The reaction of LiN(SiMe2CH2PPh2)2 with RuCl2(PPh3)3 leads to the formation of the ruthenium amide complex RuCl(PPh3)[N(SiMe2CH2PPh2)2]. This complex reacts with H2 to form two isomeric amine-hydride derivatives of the formula RuCl(PPh3)H[NH(SiMe2CH2PPh2)2]. Reaction of RuCl(PPh3)[N-(SiMe2CH2PPh2)2] with MeLi, Me3SiCH2Li, or H2C = CHCH2MgCl does not lead to the expected hydrocarbyl derivative; rather, ortho metalation occurs to generate Ru(C6H4PPh2)[N(SiMe2CH2PPh2)2]. Attempts to displace the PPh3 ligand of RuCl(PPh3)[N(SiMe2CH2PPh2)2] with PEt3 lead to the formation of RuCl(C6H4PPh2)[NH(SiMe2PPh2)2], having an amine ligand and the ortho-metalated phenyl group. The complex RuCl(C6H4PPh2)[NH(SiMe2CH2PPh2)2] crystallizes in space group P2(1)/n with a = 9.8385 (5) angstrom},
	keywords = {5-COORDINATE D6 COMPLEXES, CARBONYL-COMPLEXES, CRYSTAL, formation, HYDROGEN, IRIDIUM, MOLECULAR-STRUCTURE, STEREOSELECTIVE},
	isbn = {0276-7333},
	url = {<Go to ISI>://A1991EY68100025},
	author = {Fryzuk,Michael D. and Montgomery, C. D. and Rettig, S. J.}
}
@article {7015,
	title = {THERMAL AND PHOTOCHEMICAL-TRANSFORMATIONS OF ORGANOIRIDIUM PHOSPHIDE COMPLEXES - MECHANISTIC STUDIES ON CARBON PHOSPHORUS BOND FORMATION TO GENERATE CYCLOMETALATED HYDRIDE COMPLEXES BY ALPHA-HYDRIDE ABSTRACTION},
	journal = {Journal of the American Chemical Society},
	volume = {113},
	number = {23},
	year = {1991},
	note = {ISI Document Delivery No.: GP037Times Cited: 28Cited Reference Count: 62},
	month = {Nov},
	pages = {8724-8736},
	type = {Article},
	abstract = {{The thermal and photolytic transformations of a series of methyliridium(III) phosphide complexes are described. Complexes of the formula Ir(CH3)PR2[N(SiMe2CH2PPh2)2] (R = Ph, Me) rearrange thermally to generate the corresponding cyclometalated derivatives fac-Ir(eta-2-CH2PR2)H[N(SiMe2CH2PPh2)2]; continued thermolysis results in the formation of the iridium(I) phosphine complexes Ir(PMeR2)[N(SiMe2CH2PPh2)2]. Under photolytic conditions the phosphide derivatives rearrange directly to the phosphine complexes with no observable intermediates. The phenylphosphide complex Ir(CH3)PHPh[N-(SiMe2CH2PPh2)2] rearranges directly to the phosphine derivative Ir(PHPhMe)[N(SiMe2CH2PPh2)2] both thermally and photolytically with no observable intermediates. Crystals of lr(CH3)PPh2[N(SiMe2CH2PPh2)2] are monoclinic with a = 13.506 (3) angstrom},
	keywords = {ACTIVATION, C-H, CHEMISTRY, CRYSTAL-STRUCTURE, DERIVATIVES, HYDROGEN-BONDS, IRIDIUM, LIGAND, REACTIVITY, REDUCTIVE ELIMINATION},
	isbn = {0002-7863},
	url = {<Go to ISI>://A1991GP03700020},
	author = {Fryzuk,Michael D. and Joshi, K. and Chadha, R. K. and Rettig, S. J.}
}
