Potassium, rubidium, cesium, and barium ferrates(VI). Preparations, infrared spectra, and magnetic susceptibilities

1972 ◽  
Vol 11 (8) ◽  
pp. 1904-1908 ◽  
Author(s):  
R. J. Audette ◽  
J. W. Quail
Keyword(s):  
Infrared Spectra ◽  
Magnetic Susceptibilities

Some amine-thiocyanate complexes of nickel(II)

1966 ◽  
Vol 19 (8) ◽  
pp. 1423 ◽  
Author(s):  
NF Curtis ◽  
YM Curtis
Keyword(s):  
Infrared Spectra ◽  
Reflectance Spectra ◽  
Magnetic Susceptibilities ◽  
Thiocyanate Ion ◽  
Thiocyanate Complexes

The preparation and properties of Ni(l,3-pn)2(NCS)2, Ni(trien)(NCS)2, Ni(tet a)(NCS)2, Ni(tet b)(NCS)2, Ni(dien)(NCS)2, Ni(dpt)(NCS)2, Ni(en)2NCSClO4, and Ni(trien)NCSClO4 are described (1,3-pn = 1,3-diaminopropane, trien = triethylenetetramine, tet a and tet b are isomeric hexamethylcyclotetradecanes, dien = diethylenetriamine, dpt = dipropylenetriamine, en = ethylenediamine). The first four compounds are normal N-bonded dithiocyanato derivatives, the dien and dpt derivatives have structures with one N-bonded terminal, and one bridging thiocyanate ion, and the thiocyanate perchlorate compounds have structures with a bridging thiocyanate ion. Magnetic susceptibilities (all μeff c. 3.1 B.M.), infrared spectra (including that of N-deuterated Si(l,3-pn)2(NCS)2), reflectance spectra, and conductances in methanol and acetone are reported.

Tetracyanonickelate(II) compounds of some (tetraazamacrocycle)nickel(II) cations. The structure of catena-Di(μ-cyano)dicyano(N-meso-5,7,7,12,14,14-hexamethy1-1,4,8,11-tetraazacyclotetradeca-1, 11-diene)dinicke1(II) hydrate

1984 ◽  
Vol 37 (9) ◽  
pp. 1799 ◽  
Author(s):  
GJ Gainsford ◽  
NF Curtis
Keyword(s):  
Infrared Spectra ◽  
Ground State ◽  
Singlet Ground State ◽  
Ring Size ◽  
Triplet Ground State ◽  
Coordination Environment ◽  
Magnetic Susceptibilities ◽  
X Ray ◽  
A Chain ◽  
Tetracyanonickelate Compounds

Tetracyanonickelate(II) compounds of several (tetraazamacrocycle)nickel(II) cations have been prepared. The structure of the N-meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca- 4,11-diene, hmtd, compound [Ni(hmtd)Ni(CN)4].H2O has been determined by X-ray diffractometry [monoclinic, a 1780.3(3), b 1063.41(7), c 1409.3(2) pm, β 120.54(1)�, 24, space group C2/c, R 0.021, Rw 0.030 for 2178 reflections] and shows a chain polymeric structure with trans singlet ground state [Ni(CN)4]2- groups linking parallel stacked triplet ground state [Ni(hmtd)]2+ groups. The triplet ground state nickel(II) ions have a tetragonally elongated coordination environment [Ni-N (mean macrocycle) 204.5(1) pm, Ni-N (N≡C) 220.7(1) pm]. Tetracyanonickelate compounds of macrocycles related to hmtd but with different substituents, macrocycle ring size, and/or numbers of imine and amine donor groups were prepared. Some are diamagnetic, with discrete cation and anion, while others are similar to the hmtd compound, and for the latter, tetragonal distortions were evaluated from the reflectance spectra. Magnetic susceptibilities and infrared spectra are reported.

Coordination compounds of substituted 1,10-phenanthrolines and related bipyridyls. XI. Physicochemical study of complexes of copper(II) and 2-Methyl-1,10-phenanthroline

1970 ◽  
Vol 23 (4) ◽  
pp. 691 ◽  
Author(s):  
EW Ainscough ◽  
RA Plowman
Keyword(s):  
Organic Solvents ◽  
Infrared Spectra ◽  
Coordination Compounds ◽  
Water Solution ◽  
Sodium Perchlorate ◽  
Copper Nitrate ◽  
Visible Absorption ◽  
Magnetic Susceptibilities ◽  
Excess Copper ◽  
Donor Nitrogen

Solutions of 2-methyl-1,10-phenanthroline (rnep) with excess copper(II) salts in organic solvents yielded complexes of the formula Cu(mep)X2 (X = NO3, Cl, Br, I). These were non-electrolytes in nitrobenzene. When excess rnep was present bis- complexes of the type Cu(mep)2Cl2,6H2O, Cu(mep)2/sub>(NO3)2,H2O, and hydrated forms of the type Cu(mep)2XClO4 (X = Cl, NO3) were obtained. These were 1 : 1 electrolytes in nitrobenzene and the copper(II) ion was at least five-coordinated with the donor nitrogen atoms taking up a flattened tetrahedral arrangement. Hydrated copper(II) perchlorate with rnep in a 1 : 2 or 1 : 1 ratio yielded Cu(mep)2(ClO4)2,2H2O which is a 2 : 1 electrolyte in nitrobenzene. From a water solution of copper nitrate and rnep in the ratio 1 : 3.5, a complex Cu(mep)3(ClO>sub>4)2 precipitated upon the addition of a sodium perchlorate solution. I t was thought previously that this compound did not exist. The magnetic susceptibilities, the conductivities, and the visible, absorption, and infrared spectra of some rnep complexes have been obtained and structures are proposed from this information.

Coordination Compounds of Substituted 1,lO-Phenanthrolines and Related Dipyridyls. IV. Physicochemical Study of Complexes of Copper and 2,9-Dimethyl-1,10-phenanthroline

1963 ◽  
Vol 16 (1) ◽  
pp. 34 ◽  
Author(s):  
JR Hall ◽  
NK Marchant ◽  
RA Plowman
Keyword(s):  
Organic Solvents ◽  
Infrared Spectra ◽  
Copper Atom ◽  
Coordination Compounds ◽  
Magnetic Moments ◽  
Physicochemical Study ◽  
Magnetic Susceptibilities ◽  
Donor Nitrogen ◽  
Substituted 1

The magnetic susceptibilities, conductivities, and infrared spectra of some complexes of copper and 2,9-dimethyl-1,10-phenanthroline (dmp) have been obtained. The magnetic moments of the copper(II) compounds lie in the range 1.9 to 2.0 B.M. Complexes of formula CudmpX2, where X = NO3, Cl, and Br, are nonelectrolytes in nitrobenzene. The substances Cu(dmp)2X2H2O and hydrated forms of the compounds Cu(dmp)2XClO4, where X = NO3, Cl, and Br behave as 1 : 1 electrolytes. The copper(II) ion in the bis complexes is at least five-coordinate and it is proposed that the donor nitrogen atoms take up a flattened tetrahedral arrangement. The complexes of formula Cu(dmp)2X, where X = NO3, ClO4, Cl, Br. I, and I3 are diamagnetic solids, 1 : 1 electrolytes in nitrobenzene, and are expected to have a tetrahedral arrangement of the four donor nitrogen atoms about the copper atom. The mono complexes CudmpX, where X = Cl, Br, and I are diamagnetic, practically insoluble in organic solvents, and probably dimeric with a tetrahedral arrangement of the ligand donor atoms.

Infrared spectra of carbon monoxide on platinum, iridium and copper ; comparison of flat and rough surfaces

1981 ◽  
Vol 78 ◽  
pp. 927-932 ◽  
Author(s):  
F.J.C.M. Toolenaar ◽  
G.J. van der Poort ◽  
F. Stoop ◽  
V. Ponec
Keyword(s):  
Carbon Monoxide ◽  
Infrared Spectra ◽  
Rough Surfaces

MODELING THE CONFORMATION-SPECIFIC INFRARED SPECTRA OF N-ALKYLBENZENES

2016 ◽  
Author(s):  
Daniel Tabor ◽  
Timothy Zwier ◽  
Joseph Korn ◽  
Daniel Hewett ◽  
Edwin Sibert
Keyword(s):  
Infrared Spectra
Sign in / Sign up

Export Citation Format

Share Document