@article {4412,
	title = {Transition metal azolates from metallocenes. Part 3: Polymeric manganese(II) and nickel(II) pyrazolates; synthesis, characterization, and magnetochemistry},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {76},
	number = {8},
	year = {1998},
	note = {ISI Document Delivery No.: 143VNTimes Cited: 13Cited Reference Count: 37},
	month = {Aug},
	pages = {1130-1137},
	type = {Article},
	abstract = {Direct reactions of nickelocene and manganocene with molten pyrazoles in an inert atmosphere or under vacuum have led to the isolation of the following metal pyrazolate compounds: [Ni(4-Xpz)(2)](x) (where X = EI, CI and pz = pyrazolate); [M(4-Xdmpz)(2)](x) (where X = H, CH3, Cl, Br and M = Ni, Mn and dmpz = 3,5-dimethylpyazolate); and [Mn(4-Xpz)(2)(4-XpzH)](x) (where X = Cl, Br and pzH = pyrazole). On the basis of indirect evidence all compounds are considered to have extended chain structures with metal ions linked in chains by double bridging pyrazolates. The two [Ni(4-Xpz)2], compounds are diamagnetic while all others are paramagnetic. Variable temperature magnetic susceptibility studies on the paramagnetic compounds reveal antiferromagnetic coupling between neighbouring metal ions. Analysis of the magnetic data (Hamiltonian of the form II = -2J Sigma S-i S-j) yields values of the exchange coupling constant J of -14 to -17 cm(-1) for the [Ni(4-Xdmpz)(2)](x) compounds, -1.2 to -2.1 cm(-1) for the [Mn(4-Xdmpz)(2)](x) compounds, and -0.41 cm(-1) for the [Mn(4-Xpz)(2)(4-XpzH)](x) compounds.},
	keywords = {3, 5-DIMETHYLPYRAZOLATE, ANTIFERROMAGNETIC EXCHANGE, BR, CH3, COMPLEXES, CRYSTAL-STRUCTURE, LIGANDS, MAGNETIC-PROPERTIES, manganese, manganocene, NICKEL, nickelocene, pyrazolates, REACTIVITY},
	isbn = {0008-4042},
	url = {<Go to ISI>://000077277900003},
	author = {Storr, A. and Summers, D. A. and Thompson, R. C.}
}
@article {4412,
	title = {Transition metal azolates from metallocenes. Part 3: Polymeric manganese(II) and nickel(II) pyrazolates; synthesis, characterization, and magnetochemistry},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {76},
	number = {8},
	year = {1998},
	note = {ISI Document Delivery No.: 143VNTimes Cited: 13Cited Reference Count: 37},
	month = {Aug},
	pages = {1130-1137},
	type = {Article},
	abstract = {Direct reactions of nickelocene and manganocene with molten pyrazoles in an inert atmosphere or under vacuum have led to the isolation of the following metal pyrazolate compounds: [Ni(4-Xpz)(2)](x) (where X = EI, CI and pz = pyrazolate); [M(4-Xdmpz)(2)](x) (where X = H, CH3, Cl, Br and M = Ni, Mn and dmpz = 3,5-dimethylpyazolate); and [Mn(4-Xpz)(2)(4-XpzH)](x) (where X = Cl, Br and pzH = pyrazole). On the basis of indirect evidence all compounds are considered to have extended chain structures with metal ions linked in chains by double bridging pyrazolates. The two [Ni(4-Xpz)2], compounds are diamagnetic while all others are paramagnetic. Variable temperature magnetic susceptibility studies on the paramagnetic compounds reveal antiferromagnetic coupling between neighbouring metal ions. Analysis of the magnetic data (Hamiltonian of the form II = -2J Sigma S-i S-j) yields values of the exchange coupling constant J of -14 to -17 cm(-1) for the [Ni(4-Xdmpz)(2)](x) compounds, -1.2 to -2.1 cm(-1) for the [Mn(4-Xdmpz)(2)](x) compounds, and -0.41 cm(-1) for the [Mn(4-Xpz)(2)(4-XpzH)](x) compounds.},
	keywords = {3, 5-DIMETHYLPYRAZOLATE, ANTIFERROMAGNETIC EXCHANGE, BR, CH3, COMPLEXES, CRYSTAL-STRUCTURE, LIGANDS, MAGNETIC-PROPERTIES, manganese, manganocene, NICKEL, nickelocene, pyrazolates, REACTIVITY},
	isbn = {0008-4042},
	url = {<Go to ISI>://000077277900003},
	author = {Storr, A. and Summers, D. A. and Thompson, R. C.}
}
@article {3534,
	title = {COORDINATION POLYMERS INCORPORATING WEAKLY COORDINATING FLUOROANIONS},
	journal = {Journal of Fluorine Chemistry},
	volume = {71},
	number = {2},
	year = {1995},
	note = {ISI Document Delivery No.: QV343Times Cited: 1Cited Reference Count: 9George H Cady Symposium on Inorganic Chemistry, at the 207th Meeting of the American-Chemical-SocietyMAR 14-17, 1994SAN DIEGO, CAAMER CHEM SOC},
	month = {Apr},
	pages = {191-191},
	type = {Proceedings Paper},
	keywords = {ANTIFERROMAGNETIC EXCHANGE, coordination polymers, FLUOROANIONS, MAGNETIC EXCHANGE, SINGLE-CRYSTAL X-RAY DIFFRACTION, SYNTHESIS},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1995QV34300020},
	author = {Thompson, R. C.}
}
@article {7220,
	title = {STRUCTURE AND MAGNETIC-PROPERTIES OF MONOPHENYLPHOSPHINATE BRIDGED CHAIN POLYMERS OF MANGANESE(II), [MNL2(HPHPO2)2]X (WHERE L = HPHPO2H, CH3CONH2, H2O, HCONH(CH3), AND C5H5N)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {70},
	number = {3},
	year = {1992},
	note = {ISI Document Delivery No.: JD670Times Cited: 7Cited Reference Count: 19},
	month = {Mar},
	pages = {732-741},
	type = {Article},
	abstract = {{Crystals of Mn(CH3CONH2)2(HPhPO2)2 are monoclinic},
	keywords = {ANTIFERROMAGNETIC EXCHANGE, cobalt(II), CRYSTAL, crystal structures, MAGNETIC PROPERTIES, POLYMERIC MANGANESE MONOPHENYLPHOSPHINATES},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1992JD67000007},
	author = {Du, J. L. and Rettig, S. J. and Thompson, R. C. and Trotter, J. and Betz, P. and Bino, A.}
}
@article {7220,
	title = {STRUCTURE AND MAGNETIC-PROPERTIES OF MONOPHENYLPHOSPHINATE BRIDGED CHAIN POLYMERS OF MANGANESE(II), [MNL2(HPHPO2)2]X (WHERE L = HPHPO2H, CH3CONH2, H2O, HCONH(CH3), AND C5H5N)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {70},
	number = {3},
	year = {1992},
	note = {ISI Document Delivery No.: JD670Times Cited: 7Cited Reference Count: 19},
	month = {Mar},
	pages = {732-741},
	type = {Article},
	abstract = {{Crystals of Mn(CH3CONH2)2(HPhPO2)2 are monoclinic},
	keywords = {ANTIFERROMAGNETIC EXCHANGE, cobalt(II), CRYSTAL, crystal structures, MAGNETIC PROPERTIES, POLYMERIC MANGANESE MONOPHENYLPHOSPHINATES},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1992JD67000007},
	author = {Du, J. L. and Rettig, S. J. and Thompson, R. C. and Trotter, J. and Betz, P. and Bino, A.}
}
