@article {2408,
	title = {Tantalum-Amidate Complexes for the Hydroaminoalkylation of Secondary Amines: Enhanced Substrate Scope and Enantioselective Chiral Amine Synthesis},
	journal = {Angewandte Chemie-International Edition},
	volume = {48},
	number = {44},
	year = {2009},
	note = {ISI Document Delivery No.: 513DPTimes Cited: 9Cited Reference Count: 25Eisenberger, Patrick Ayinla, Rashidat O. Lauzon, Jean Michel P. Schafer, Latcrel L.},
	pages = {8361-8365},
	type = {Article},
	keywords = {ALKENES, ALKYLATION, alpha, amidates, BOND, C-H ACTIVATION, CATALYSIS, CATALYTIC HYDROAMINOALKYLATION, enantioselectivity, homogeneous, HYDROAMINATION, HYDROAMINOALKYLATION, IMINE, LIGANDS, tantalum, UNACTIVATED OLEFINS},
	isbn = {1433-7851},
	url = {<Go to ISI>://000271302900038},
	author = {Eisenberger, P. and Ayinla, R. O. and Lauzon, J. M. P. and Schafer, L. L.}
}
@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 {377,
	title = {Cyclohexadienyl niobium complexes and arene hydrogenation catalysis},
	journal = {Organometallics},
	volume = {21},
	number = {23},
	year = {2002},
	note = {ISI Document Delivery No.: 612WDTimes Cited: 6Cited Reference Count: 45},
	month = {Nov},
	pages = {5047-5054},
	type = {Article},
	abstract = {Hydrogenolysis of (R)[P2N2]NbCH2SiMe3 (where (R)[P2N2] = RP(CH2SiMe2NSiMe2CH2)(2)PR; R = cyclohexyl, Cy, or phenyl, Ph) in benzene or toluene causes hydride addition to the aromatic solvent resulting in the formation of the pi-bonded complexes (R)[P2N2]Nb(eta(5)-C6H7) (R = Cy, 1; R = Ph, 2) and (R)[P2N2]Nb(eta(5)-C7H9) (R = Cy, 3; R = Ph, 4) in benzene and toluene, respectively. Performing the hydrogenation at a higher pressure of 29 atm at room temperature causes the catalytic hydrogenation of benzene to cyclohexane as determined by NMR spectroscopy and GC-MS analysis. The hydrogenation of toluene to methylcyclohexane can also be performed, but the turnover frequency is considerably lower. Examination of the solid residues from the high-pressure hydrogenations indicates the formation of the pi-bonded complexes 1 and 2. The additionof 29 atm of H-2 to these cyclohexadienyl derivatives in benzene or toluene, however, shows no hydrogenation products, indicating these species are not catalytically active.},
	keywords = {AROMATIC-HYDROCARBONS, BOND, CHEMISTRY, CRYSTAL-STRUCTURE, HOMOGENEOUS HYDROGENATION, LIGANDS, TANTALUM DIHYDRIDE},
	isbn = {0276-7333},
	url = {<Go to ISI>://000179097700024},
	author = {Fryzuk,Michael D. and Kozak, C. M. and Bowdridge, M. R. and Patrick, B. O.}
}
@article {5077,
	title = {Macrocyclic complexes of niobium(III): Synthesis, structure, and magnetic behavior of mononuclear and dinuclear species that incorporate the [P2N2] system},
	journal = {Organometallics},
	volume = {20},
	number = {17},
	year = {2001},
	note = {ISI Document Delivery No.: 464CMTimes Cited: 12Cited Reference Count: 72},
	month = {Aug},
	pages = {3752-3761},
	type = {Article},
	abstract = {{The coordination chemistry of the two mixed donor macrocyclic ligands (R)[P2N2] (where (R)[P2N2] = RP(CH2SiMe2NSiMe2CH2)(2)PR},
	keywords = {= PHP(CH2SIME2NSIME2CH2)(2)PPH, AMIDE, ARENE HYDROGENATION, BOND, C-H, CRYSTAL-STRUCTURES, DERIVATIVES, MOLECULAR-STRUCTURE, N BOND-CLEAVAGE, TRIPLE, X-ray structures},
	isbn = {0276-7333},
	url = {<Go to ISI>://000170515600024},
	author = {Fryzuk,Michael D. and Kozak, C. M. and Bowdridge, M. R. and Jin, W. C. and Tung, D. and Patrick, B. O. and Rettig, S. J.}
}
@article {5157,
	title = {The nitrous oxide complex, RuCl2(eta(1)-N2O)(P-N)(PPh3) (P-N = [o-(N,N-dimethylamino)phenyl]diphenylphosphine); Low temperature conversion of N2O to N-2 and O-2},
	journal = {Journal of the American Chemical Society},
	volume = {123},
	number = {35},
	year = {2001},
	note = {ISI Document Delivery No.: 467XNTimes Cited: 22Cited Reference Count: 62},
	month = {Sep},
	pages = {8596-8597},
	type = {Article},
	keywords = {3-COORDINATE MOLYBDENUM(III), ADSORBED N2O, BOND, CRYSTAL-STRUCTURE, DECOMPOSITION, LEWIS ACIDITY, N-15 NMR, OXYGEN-ATOM TRANSFER, REACTIVITY, REDUCTASE},
	isbn = {0002-7863},
	url = {<Go to ISI>://000170729200019},
	author = {Pamplin, C. B. and Ma, E. S. F. and Safari, N. and Rettig, S. J. and James, Brian R.}
}
@article {4561,
	title = {Reaction of diphenylborinic acid with pyridinium and phosphonium bisacyl methylides. Crystal and molecular structures of resulting B,N- and B,P-betaines},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {77},
	number = {4},
	year = {1999},
	note = {ISI Document Delivery No.: 204JXTimes Cited: 8Cited Reference Count: 27},
	month = {Apr},
	pages = {439-450},
	type = {Article},
	abstract = {{Reaction of pyridinium and phosphonium 2-carboxy-1-formyl-2-oxoethylides with oxybis(diphenylborane) yields 5-(2-oxo-1-(pyridinio or phosphonio)ethylidene)-2,2-diphenyl-1,3-dioxa-2-borata-4-cyclopentanones , which represent novel types of boron nitrogen and boron phosphorus betaines, respectively. Crystals of 5-(2-oxo-1-pyridinioethylidene)-2,2-diphenyl-1,3-dioxa-2-borata-4-cyclop entanone, 1a, are monoclinic},
	keywords = {bisacyl methylide diphenylboron, BOND, BORON, boron nitrogen betaines, boron phosphorus betaines, Chelates, crystal structures, ORGANOBORON COMPOUNDS, phosphonium ylides, pyridinium ylides},
	isbn = {0008-4042},
	url = {<Go to ISI>://000080762100005},
	author = {Grunefeld, J. and Kliegel, W. and Rettig, S. J. and Trotter, J.}
}
@article {3611,
	title = {Syntheses and vibrational and C-13 MAS-NMR spectra of bis(carbonyl)mercury(II) undecafluorodiantimonate(V) ([Hg(CO)(2)][Sb2F11](2)) and of bis(carbonyl) dimercury(I) undecafluorodiantimonate ([Hg-2(CO)(2)][Sb2F11](2)) and the molecular structure of [Hg(CO},
	journal = {Inorganic Chemistry},
	volume = {35},
	number = {1},
	year = {1996},
	note = {ISI Document Delivery No.: TP072Times Cited: 53Cited Reference Count: 96},
	month = {Jan},
	pages = {82-92},
	type = {Article},
	abstract = {The synthesis of bis(carbonyl)mercury(II) undecafluorodiantimonate(V), [Hg(CO)(2)][Sb2F11](2), and that of the corresponding mercury(I) salt [Hg-2(CO)(2)][Sb2F11](2) are accomplished by the solvolyses of Hg(SO3F)(2) or of Hg2F2, treated with fluorosulfuric acid, HSO3F, in liquid antimony(V) fluoride at 80 or 60 degrees C, respectively, in an atmosphere of CO (500-800 mbar). The resulting white solids are the first examples of metal carbonyl derivatives formed by a post-transition element. Both salts are characterized by FT-IR, FT-Raman, and C-13-MAS-NMR spectroscopy. For [Hg(CO)(2)][Sb2F11], unprecedentedly high CO stretching frequencies (<(nu)over bar>(av) = 2279.5 cm(-1)) and stretching force constant (f(r) = 21.0 +/- 0.1) x 10(2) Nm(-1)) are obtained. Equally unprecedented is the (1)J(C-13-Hg-199) value of 5219 +/- 5 Hz observed in the C-13 MAS-NMR spectrum of the C-13 labeled isotopomers at delta = 168.8 +/- 0.1 ppm. The corresponding values (<(nu)over bar>(av) = 2247 cm(-1), f(r) = (20.4 +/- 0.1) x 10(2) Nm(-1), (1)J(C-13-Hg-199) = 3350 +/- 50 Hz and (2)J(C-13-Hg-199) 850 +/- 50 Hz) are found for [Hg-2(CO)(2)][Sb2F11](2), which has lower thermal stability (decomposition point in a sealed tube is 140 degrees C vs 160 degrees C for the Hg(II) compound) and a decomposition pressure of 8 Torr at 20 degrees C. The mercury(I) salt is sensitive toward oxidation to [Hg(CO)(2)][Sb2F11](2) during synthesis. Both linear cations (point group D infinity h) are excellent examples of nonclassical (sigma-only) metal-CO bonding. Crystal data for [Hg(CO)(2)][Sb2F11](2): monoclinic, space group P2(1)/n; Z = 2; a = 7.607(2) Angstrom; b = 14.001(3) Angstrom; c = 9.730(2) Angstrom; beta = 111.05(2)degrees; V = 957.1 Angstrom(3); T = 195 K; R(F) = 0.035 for 1983 data (I-0 greater than or equal to 2.5 sigma(I-0)) and 143 variables. The Hg atom lies on a crystallographic inversion center. The Hg-C-O angle is 177.7(7)degrees. The length of the mercury-carbon bond is 2.083(10) Angstrom and of the C-O bond 1.104(12) Angstrom respectively. The structure is stabilized in the solid state by a number of significant secondary interionic Hg{\textendash}-F and C{\textendash}-F contacts.},
	keywords = {ACIDS, BOND, CARBON-MONOXIDE, CATIONS, CONSTANTS, CRYSTAL-STRUCTURES},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1996TP07200016},
	author = {Bodenbinder, M. and Balzerjollenbeck, G. and Willner, H. and Batchelor, R. J. and Einstein, F. W. B. and Wang, C. and Aubke, F.}
}
@article {3420,
	title = {SPONTANEOUS ISOMERIZATION OF SYMMETRICAL M(MU-NO)(2)M LINKAGES TO (ON)M=N=M=O GROUPINGS},
	journal = {Journal of the American Chemical Society},
	volume = {117},
	number = {34},
	year = {1995},
	note = {ISI Document Delivery No.: RR735Times Cited: 13Cited Reference Count: 50},
	month = {Aug},
	pages = {8798-8806},
	type = {Article},
	abstract = {{Treatment of Cp*Mo(NO)R(2) complexes (Cp* = eta(5)-C(5)Me(5); R = CH(2)CMe(3), CH(2)CMe(2)Ph) in C6H6 at 5 degrees C with H-2 results in the formation of [Cp*MoR](2)(mu-NO)(2) products (R = CH(2)CMe(3) (1), CH(2)CMe(2)Ph (2)) which are isolable in 25-30\% yields. Similar treatment of an equimolar mixture of Cp*Mo(NO)(CH(2)SiMe(3))(2) and Cp*W(NO)(CH(2)SiMe(3))(2) with H-2 results in the formation of a heterobimetallic species, [Cp*Mo(CH(2)SiMe(3))](mu-NO)(2)[Cp*W(CH(2)SiMe(3))] (3). Complexes 1, 2, and 3 isomerize in solution at ambient temperatures To form [Cp*Mo-(NO)R](mu-N)[Cp*Mo(O)R] (R = CH(2)CMe(3) (4), CH(2)CMe(2)Ph (5)) and a 60:40 (M(1) = W:M(1) = Mo) mixture of [Cp*M(1)(NO)(CH(2)SiMe(3))](mu-N)[Cp*M(2)(O)(CH(2)SiM(3))] (6), respectively. The solid-state molecular structures of 1 and 6 have been established by single-crystal X-ray crystallographic analyses. Crystals of [Cp*Mo(CH(2)CMe(3))](2)-(mu-NO)(2) (1) are orthorhombic of space group Pbcn: a = 12.570(3) Angstrom},
	keywords = {(ETA-5-C5ME5)RU(NO), BOND, COMPLEXES, GAS-PHASE, LIGANDS, MOLYBDENUM, NITRIC-OXIDE, ORGANOMETALLIC NITROSYL CHEMISTRY, OXIDATIVE ADDITION-REACTIONS, TUNGSTEN},
	isbn = {0002-7863},
	url = {<Go to ISI>://A1995RR73500013},
	author = {Legzdins,Peter and Young, M. A. and Batchelor, R. J. and Einstein, F. W. B.}
}
@article {3031,
	title = {MAGNETIC EXCHANGE IN DINUCLEAR CHROMIUM(II) COMPLEXES - EFFECT OF BRIDGING CHLORIDES AND BRIDGING HYDRIDES IN ANTIFERROMAGNETIC COUPLING},
	journal = {Inorganic Chemistry},
	volume = {33},
	number = {24},
	year = {1994},
	note = {ISI Document Delivery No.: PU080Times Cited: 24Cited Reference Count: 33},
	month = {Nov},
	pages = {5528-5534},
	type = {Article},
	abstract = {{The preparation, solid-state structures, and magnetic properties of two new Cr(II) amido diphosphine complexes are described. Reaction of the lithium salt LiN(SiMe(2)CH(2)PPh(2))(2) with CrCl2.THF results in the formation of the dinuclear chloride-bridged species {[(Ph(2)PCH(2)SiMe(2))(2)N]Cr}(2)(mu-Cl)(2), 1. This complex is paramagnetic at room temperature with a magnetic moment corresponding to four unpaired electrons per chromium; however, as the temperature is lowered, magnetic susceptibility measurements show that 1 exhibits antiferromagnetic behavior with J = -12.4 cm(-1) and g = 1.99. Chloride 1 can be converted to the mononuclear methyl complex CrMe[N(SiMe(2)CH(2)PPh(2))(2)] by reaction with MeLi. Under a hydrogen atmosphere, the methyl complex is converted to the dinuclear hydride derivative {[(Ph(2)PCH(2)SiMe(2))(2)N]Cr}(2)(mu-H)(2), 3. A variable temperature magnetic susceptibility study shows that this species is very strongly antiferromagnetically coupled with J = -139 cm(-1) and g = 1.98. The magnetic coupling correlates with the Cr-Cr distances observed in the solid state for these complexes: for 1, the Cr-Cr distance is 3.64 while for the hydride 3 a much shorter distance of 2.641 Angstrom is found. Crystals of {[(Ph(2)PCH(2)SiMe(2))(2)N]Cr}(2)(mu-Cl)(2), 1, are triclinic},
	keywords = {BOND, CR, CRYSTAL-STRUCTURES},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1994PU08000029},
	author = {Fryzuk,Michael D. and Leznoff, D. B. and Rettig, S. J. and Thompson, R. C.}
}
@article {2773,
	title = {PREPARATION AND CHARACTERIZATION OF THE OSMIUM CLUSTER COMPLEXES H2OS3(CO)8L(ETFCPCME) (L=CO OR PET2FC) AND H2OS3(CO)8[(ETA-C5H3PET2)FE(ETA-C5H4)]},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {71},
	number = {3},
	year = {1993},
	note = {ISI Document Delivery No.: KU982Times Cited: 4Cited Reference Count: 35},
	month = {Mar},
	pages = {399-409},
	type = {Article},
	abstract = {{Thermolysis of Os3(CO)11](PEt2Fc) (Fc = (eta-C5H4)Fe(eta-C5H5)) in octane for 8 h affords H2Os3(CO)9(EtFcPCMe), 10, and H2Os3(CO)8[(eta-C5H3PEt2)Fe(eta-C5H4)], 9e, in 15 and 65\% yield, respectively. Heating Os3(CO),2 and PEt2Fc in 1:2 molar ratio in xylene for 10 h gives two isomers of H2Os3(CO)8(PEt2Fc)(EtFcPCMe), 11, in about 40\% yield. Two crystalline modifications of the complex 9e have been obtained from the same solvent: 9eA, triclinic},
	keywords = {BENZYNE, BOND, CHEMISTRY, COMPOUND, COORDINATION, LIGANDS, MODE, RAY CRYSTAL-STRUCTURES, REACTIVITY, TRIOSMIUM CLUSTERS},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1993KU98200020},
	author = {Cullen, W. R. and Rettig, S. J. and Zheng, T. C.}
}
@article {7251,
	title = {BIS(DIPHENYLPHOSPHINO)METHANE COMPLEXES OF PALLADIUM AS CATALYSTS FOR HYDROSILYLATION OF OLEFINS BY TRICHLOROSILANE},
	journal = {Journal of Molecular Catalysis},
	volume = {72},
	number = {2},
	year = {1992},
	note = {ISI Document Delivery No.: HT940Times Cited: 5Cited Reference Count: 22},
	month = {Mar},
	pages = {167-171},
	type = {Article},
	abstract = {Mononuclear Pd(II), and dinuclear Pd(O) and Pd(I) complexes containing bis(diphenylphosphino)methane catalyze the addition of trichlorosilane to the olefinic bond of hexene-1, styrene and vinyltrichlorosilane. Activity relationships for limited data at 80 and 120-degrees-C suggest that in each case mononuclear Pd(O) species might act as a catalyst precursor.},
	keywords = {BOND, CRYSTAL, HYDROGEN-SULFIDE, INSERTION, metal complexes, Pd(I), PHOSPHINE COMPLEXES},
	isbn = {0304-5102},
	url = {<Go to ISI>://A1992HT94000006},
	author = {Gulinski, J. and James, Brian R.}
}
@article {7253,
	title = {MOLECULAR DIHYDROGEN AND HYDRIDO DERIVATIVES OF RUTHENIUM(II) COMPLEXES CONTAINING CHELATING FERROCENYL-BASED TERTIARY PHOSPHINE AMINE LIGANDS AND OR MONODENTATE TERTIARY PHOSPHINE-LIGANDS},
	journal = {Inorganic Chemistry},
	volume = {31},
	number = {26},
	year = {1992},
	note = {ISI Document Delivery No.: KE754Times Cited: 34Cited Reference Count: 60},
	month = {Dec},
	pages = {5509-5520},
	type = {Article},
	abstract = {{Reactions of complexes of the type RuCl2(PPh3)(P-N) with H2 are reported, where P-N represents the chelating ferrocene-based ligands (eta-C5H5)Fe(etaC5H3(CHMeNMe2)PR2-1,2) with R = i-Pr (the isoPFA ligand) or Ph (the PPFA ligand). Depending on the solvent(s) used, and absence or presence of added base, RuCl2(PPh3)(isoPFA) (2b) generates the dinuclear eta2-H2 complexes L2(eta2-H2)Ru(eta-Cl)2(eta-H)Ru(H)(PPh3)2 where L2 = isoPFA (complex 3) or L2 = (PPh3)2 (complex 4). n-Butanol solutions of RuCl2(PPh3)(PPFA) (2a) under H-2 also yield 4, as well as Ru(H)Cl2(PPh3)(PPFA.H)(BuOH), a zwitterionic species containing a protonated amine moiety stabilized by coordinated n-BuOH, which is a likely intermediate in heterolytic cleavage of the H-2: the complex RuH(Cl)-PPh3)(isoPFA) (5), together with a hydrido carbonyl species, is isolated from methanol solutions of 2b. Complexes 2b, 3, 4, and 5 are characterized by X-ray crystallography; the mononuclear complexes 2b and 5 are orthorhombic with space groups F2dd and P2(2)2(1)2(1), respectively. For 2b},
	keywords = {BOND, CARBONYL, D6 COMPLEXES, ETA-2-DIHYDROGEN, EXCHANGE, H-H, HYDROGEN COMPLEXES, palladium, REACTIVITY, TRANSITION-METALS},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1992KE75400029},
	author = {Hampton, Crsm and Butler, I. R. and Cullen, W. R. and James, Brian R. and Charland, J. P. and Simpson, J.}
}
@article {7197,
	title = {SOLID-STATE P-31 NMR INVESTIGATIONS OF UNSATURATED PHOSPHORUS NITROGEN SULFUR RINGS},
	journal = {Magnetic Resonance in Chemistry},
	volume = {30},
	number = {12},
	year = {1992},
	note = {ISI Document Delivery No.: KA993Times Cited: 3Cited Reference Count: 20},
	month = {Dec},
	pages = {1220-1223},
	type = {Article},
	abstract = {Solid-state CP/MAS P-31 NMR spectra were measured for the following unsaturated phosphorus-nitrogen-sulfur ring systems: 1,5-R4P2N4S2 (R = Me, Et, Ph), 1,5-Ph4P2N4S2Ph2, Ph2PN4S3NPPH3 and Ph2PN3S2. The isotropic solid-state shifts correlate well with the corresponding shifts in solution, the largest difference being 9.0 ppm, indicating that there are no phase-dependent structural features. Analysis of the principal elements of the shielding tensor by the spinning side band method showed that one of these elements is primarily responsible for the anomalously low-field isotropic chemical shifts of 1,5-R4P2N4S2, but no correlation was found between this individual tensor component and any of the structural parameters of these folded eight-membered rings. Two isotropic shifts were observed for the crystallographically inequivalent phosphorus atoms of 1,5-Et4P2N4S2, but the individual P-31 isotropic shifts of 1,5-Me4P2N4S2 were not resolved.},
	keywords = {1, 5-DIPHOSPHADITHIATETRAZOCINES, BOND, CRYSTAL, ELECTRONIC-STRUCTURES, MAGIC ANGLE, PHOSPHORUS NITROGEN SULFUR RINGS, SOLID-STATE P-31 NMR, SPECTROSCOPY},
	isbn = {0749-1581},
	url = {<Go to ISI>://A1992KA99300010},
	author = {Chivers, T. and Edwards, M. and Fyfe, C. A. and Randall, L. H.}
}
@article {7128,
	title = {CRYSTAL-STRUCTURE AND PHOTOCHEMISTRY OF A METHYL PHENYL DIESTER DERIVATIVE OF DIBENZOBARRELENE},
	journal = {Acta Crystallographica Section C-Crystal Structure Communications},
	volume = {47},
	year = {1991},
	note = {ISI Document Delivery No.: FJ773Times Cited: 1Cited Reference Count: 17Part 4},
	month = {Apr},
	pages = {793-797},
	type = {Article},
	abstract = {{Methyl phenyl dibenzobarrelene-2,3-dicarboxylate, C25H18O4, M(r) = 382.42, monoclinic, P2(1)/c},
	keywords = {BOND, CYCLOPROPANE, GEOMETRY, SMALL RINGS, SOLID-STATE PHOTOCHEMISTRY},
	isbn = {0108-2701},
	url = {<Go to ISI>://A1991FJ77300037},
	author = {Trotter, J. and Wireko, F. C.}
}
@article {7029,
	title = {AN UNUSUAL 17-ELECTRON ORGANOMETALLIC RADICAL, CPCR(NO)(PPH3)(CH2SIME3)},
	journal = {Journal of the American Chemical Society},
	volume = {113},
	number = {18},
	year = {1991},
	note = {ISI Document Delivery No.: GD306Times Cited: 10Cited Reference Count: 18},
	month = {Aug},
	pages = {7049-7050},
	type = {Note},
	keywords = {BOND, COMPLEXES, NITROSYL CHEMISTRY, REACTIVITY},
	isbn = {0002-7863},
	url = {<Go to ISI>://A1991GD30600060},
	author = {Herring, F. G. and Legzdins,Peter and McNeil, W. S. and Shaw, M. J. and Batchelor, R. J. and Einstein, F. W. B.}
}
