Hydrogen Bonding to Transition Metal Fluoride Ligands:  The Synthesis and Structure of the Bifluoride Complex Mo(PMe3)4H2F(FHF)

1996 ◽  
Vol 118 (31) ◽  
pp. 7428-7429 ◽  
Author(s):  
Vincent J. Murphy ◽  
Tony Hascall ◽  
Johnny Y. Chen ◽  
Gerard Parkin
Keyword(s):  
Hydrogen Bonding ◽  
Transition Metal ◽  
Metal Fluoride ◽  
Fluoride Ligands

Exchange Coupling of Transition-Metal Ions through Hydrogen Bonding:  A Theoretical Investigation

2002 ◽  
Vol 124 (18) ◽  
pp. 5197-5205 ◽  
Author(s):  
Cédric Desplanches ◽  
Eliseo Ruiz ◽  
Antonio Rodríguez-Fortea ◽  
Santiago Alvarez
Keyword(s):  
Hydrogen Bonding ◽  
Transition Metal ◽  
Metal Ions ◽  
Theoretical Investigation ◽  
Exchange Coupling ◽  
Transition Metal Ions

Synthesis, crystal structure, hydrogen bonding and spectroscopy of transition-metal complexes with the ligand (N,N′-bis(2-pyridylmethyl)-1,3-propanediamine)

Polyhedron ◽  
2009 ◽  
Vol 28 (14) ◽  
pp. 2813-2820 ◽  
Author(s):  
Aminou Mohamadou ◽  
Gerard A. van Albada ◽  
Ilpo Mutikainen ◽  
Urho Turpeinen ◽  
Jérôme Marrot ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes

Structural and spectroscopic studies of transition metal nitrite complexes. V. Crystal structures and spectra of trans-Tetrakis(pyridine)dinitritonickel(II)-pyridine (1/2), trans-Tetrakis(4-methylpyridine)dinitritonickel(II) and trans-Tetrakis(pyrazole)-dinitritonickel(II)

1981 ◽  
Vol 34 (10) ◽  
pp. 2095 ◽  
Author(s):  
AJ Finney ◽  
MA Hitchman ◽  
CL Raston ◽  
GL Rowbottom ◽  
BW Skelton ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Transition Metal ◽  
Crystal Structures ◽  
Electronic Spectra ◽  
Spectroscopic Studies ◽  
Molecular Structures ◽  
Aromatic Rings ◽  
Paddle Wheel ◽  
Crystal And Molecular Structures ◽  
Infrared Frequencies

The crystal and molecular structures of the compounds [Ni(py)4(ONO)2],2py, [Ni(γmpy),(ONO)2] and [Ni(prz)4(ONO)2] are reported.�All three are trans nitrito complexes, the pyridine (py) compound containing two pyridine molecules of solvation. The aromatic rings in the first two complexes adopt 'paddle wheel' conformations with pitch angles varying between 40 and 70�. The nitrite ions are positioned so as to minimize repulsive interactions with the amines, and it seems likely that these groups bond through oxygen rather than nitrogen because this allows a lesser degree of interligand steric interference. The amine rings in [Ni(prz)4(ONO)2] are orthogonal to the plane containing the nickel and coordinated pyrazole nitrogen atoms; the nitrito groups are disordered between two inequivalent positions, each of which involves hydrogen bonding with the pyrazole NH groups. The nitrite infrared frequencies are similar to those observed for other nickel(II) nitrito complexes except that the antisymmetric NO stretching mode of one of the groups in the pyrazole complex is much lower in energy than expected, being in the range normally associated with a nitrogen-bonded or chelated nitrite group. It is suggested that this deviation may be caused by the hydrogen bonding in the complex. The electronic spectra of the compounds yield 10Dq values of 9100 and 8500 cm-1 for the nitrite ligands in [Ni(py)4(ONO)2] and Ni(prz)4(ONO)2], respectively, placing the nitrito group towards the weaker end of the spectro-chemical series.

scholarly journals Mixed Ligand Complexes of Transition Metal Ions with Selective Bio-Ligands in Surfactant-Water Mixtures

2019 ◽  
Vol 8 (2S11) ◽  
pp. 3182-3190
Keyword(s):  
Hydrogen Bonding ◽  
Transition Metal ◽  
Metal Ions ◽  
Chemical Speciation ◽  
Transition Metal Ions ◽  
Ternary Complexes ◽  
Mixed Ligand ◽  
Stacking Interactions ◽  
Micellar Media ◽  
Chelate Effect

Chemical speciation of ternary complexes of L-arginine and L-aspartic acid with essential transition metal ions was studied pH metrically. The following MLX, MLXH and ML2X ternary species are detected and reported in this paper. The existence of different ternary species is established from modeling studies using the computer program MINIQUAD75. The relative concentrations (M: L: X=1:2:2, 1:2:4, 1:4:2) and stabilities of the ternary species are compared with those of binary species. The extra stability associated with the ternary complexes is attributed to factors such as charge neutralization, chelate effect, stacking interactions and hydrogen bonding. Trend in variation of stability constants with the change in the mole fraction of the surfactant in various micellar media is explained on the basis of electrostatic and non-electrostatic forces. Distribution diagrams in relation to pH and plausible structures were presented.

Synthesis of a series of M(ii) (M = Mn, Fe, Co) chloride complexes with both inter- and intra-ligand hydrogen bonding interactions

2021 ◽  
Vol 50 (35) ◽  
pp. 12088-12092
Author(s):  
Clare A. Leahy ◽  
Michael J. Drummond ◽  
Josh Vura-Weis ◽  
Alison R. Fout
Keyword(s):  
Hydrogen Bonding ◽  
Transition Metal ◽  
Intramolecular Hydrogen Bonding ◽  
Metal Chloride ◽  
Chloride Complexes ◽  
Hydrogen Bonding Interactions ◽  
Transition Metal Chloride ◽  
Hydrogen Bonding Networks ◽  
Intramolecular Hydrogen

Hydrogen bonding networks are vital for metallo-enzymes to function; however, modeling these systems is non-trivial. The development of 1st-row transition metal chloride complexes with intramolecular hydrogen-bonding interactions are detailed herein.

Heavy Metal Fluoride Glasses for Optical Applications

1985 ◽  
Vol 61 ◽  
Author(s):  
W. A. Sibley ◽  
D. C. Yeh ◽  
Y. Suzuki ◽  
G. J. Quarles ◽  
R. C. Powell
Keyword(s):  
Heavy Metal ◽  
Rare Earth ◽  
Transition Metal ◽  
Optical Communication ◽  
Transition Metal Ions ◽  
Metal Fluoride ◽  
Fluoride Glasses ◽  
Heavy Metal Fluoride ◽  
Heavy Metal Fluoride Glasses ◽  
Light Guides

ABSTRACTGreat progress has been made in optical device technology over the past decade. This progress brings a host of new services which include voice, data and visual communications. The realization of low loss optical fibers which give rise to long distance optical communication and the growth in information processing through computer technology will lead to an accelerating growth in the utilization of light guides and light wave communication systems. Heavy metal fluoride glasses have proved to be excellent hosts for both rare earth and 3d transition metal ions. In addition, their potential as light guides is at present unexcelled. This glass is especially promising for optical display devices, laser hosts, and electroluminescence panels. Numerous defects and impurities can be incorporated in the glass which absorb or emit light. Through optical studies of rare earth ions such as Er3+, Ho3+, Nd3+ and Pr3+ it is possible to investigate the multiphonon emission rate for optical transitions in the heavy metal fluoride materials. It is found that these particular materials have a much lower multiphonon rate than oxide glasses. This makes them attractive for room temperature devices. When 3d transition metal ions are incorporated into heavy metal fluoride glasses, the optical properties are similar in many cases to those in crystals. Inhomogeneous broadening of the absorption and emission bands occurs in the glass, but the lifetimes and oscillator strengths of the transitions in glass and crystals are of the same magnitude. Radiation damage of glasses can be detrimental to long range optical communication. It is found that the heavy metal fluoride glasses damage by the photochemical mechanism which is also dominant in highly ionic materials. Optical absorption and electron spin resonance measurements have been utilized to identify the types of radiation induced defects in these materials.

New Coordination Polymers Based On Transition Metal Squarates And Pyrazine Ligands

2003 ◽  
Vol 58 (1) ◽  
pp. 52-58 ◽  
Author(s):  
Christian Näther ◽  
Jan Greve ◽  
Inke Jeß
Keyword(s):  
Hydrogen Bonding ◽  
Transition Metal ◽  
Coordination Polymers ◽  
Hydrothermal Reaction ◽  
Squaric Acid ◽  
Water Molecules ◽  
Complex Behaviour ◽  
Metal Atoms ◽  
Linear Chains ◽  
Distorted Octahedra

Abstract Three new coordination polymers have been prepared by hydrothermal reaction of squaric acid, pyrazine and the metal halides FeCl2 · 4H2O, CoBr2 and NiBr2. In their crystal structures the metal atoms are coordinated by four water molecules and two pyrazine ligands within slightly distorted octahedra. The pyrazine ligands connect the metal atoms via μ-N,N’-coordination to linear chains which are connected via hydrogen bonding. The squarate dianions are not coordinated to the metal atoms and are located between the chains. The thermal behaviour of all compounds was investigated using TG-DTA-MS measurements. A complex behaviour for all compounds is found and the decomposition temperatures increase from Fe to Ni. From these investigations there are no hints for the occurrence of stoichiometric intermediate compounds.

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