Synthesis, Crystal Structure and Spectroscopic Studies of New Charge Transfer Compounds Obtained by Reaction of TTF and the Polyoxoanion [Mo6O19]2−

1989 ◽  
Vol 173 ◽  
Author(s):  
C. Bellitto ◽  
D. Attanasio ◽  
M. Bonamico ◽  
V. Fares ◽  
P. Imperatori ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electrical Conductivity ◽  
Charge Transfer ◽  
Room Temperature ◽  
Mixed Valence ◽  
Spectroscopic Studies ◽  
Chemical Formula ◽  
Xps Spectra ◽  
Radical Cation Salts ◽  
A Chain

ABSTRACTTwo different tetrathiafulvalene radical cation salts of the [M06O19]2−polyoxoanion have been isolated and characterized. Compound 1 corresponds to the chemical formula (TTF)3[Mo6019]. The crystal structure shows a ID stack of the donor TTF molecule, and each stack fits into channels formed by the anions. Within the stack a chain of trimers is identified, the inter-trimeric distance being 3.51 Å. The I.R., electronic and XPS spectra suggest the compound to be a mixed-valence salt. The electrical conductivity at room temperature is σ = 10−4Ω−1cm−1Compound 2 corresponds to the chemical+formula (TTF)2[M06019] . The compound consists of isolated (TTF+•)2dimers, interspersed with the polyoxoanions. In agreement with this crystal structure the compound is a diamagnetic insulator.

CRYSTAL STRUCTURE, ELECTRICAL CONDUCTIVITY AND THERMAL EXPANSION OF Pr1-xSrxFeO3-δ(0 ≤ x ≤ 0.6)

2012 ◽  
Vol 26 (32) ◽  
pp. 1250174 ◽  
Author(s):  
V. PRASHANTH KUMAR ◽  
Y. S. REDDY ◽  
P. KISTAIAH ◽  
C. VISHNUVARDHAN REDDY
Keyword(s):  
Crystal Structure ◽  
Electrical Conductivity ◽  
Thermal Expansion ◽  
Room Temperature ◽  
Small Polaron ◽  
Linear Thermal Expansion ◽  
Lattice Parameter ◽  
Polaron Hopping ◽  
X Ray ◽  
Perovskite Type

The crystal structure at room temperature (RT), thermal expansion from RT to 1000°C and electrical conductivity, from RT to 600°C, of the perovskite-type oxides in the system Pr 1-x Sr x FeO 3(x = 0, 0.2, 0.4, 0.6) were studied. All the compounds have the orthorhombic perovskite GdFeO 3-type structure with space group Pbnm. The lattice parameters were determined by X-ray powder diffraction. The Pseudo cubic lattice parameter decreases with an increase in x, while the coefficient of linear thermal expansion increases. The thermal expansion is almost linear for x = 0 and 0.2. The electrical conductivity increases with increasing x while the activation energy decreases. The electrical conductivity can be described by the small polaron hopping conductivity model.

scholarly journals Electrical conductivity in two mixed-valence liquids

2015 ◽  
Vol 17 (21) ◽  
pp. 14107-14114 ◽  
Author(s):  
Wenzhi Yao ◽  
Steven P. Kelley ◽  
Robin D. Rogers ◽  
Thomas P. Vaid
Keyword(s):  
Electrical Conductivity ◽  
Electron Transfer ◽  
Exchange Rate ◽  
Rate Constants ◽  
Room Temperature ◽  
Mixed Valence ◽  
Electrical Current ◽  
Active Species ◽  
Redox Active

Two mixed-valence room-temperature liquids are reported: BuFc–[BuFc+][NTf2−] (BuFc = n-butylferrocene) and TEMPO–[TEMPO+][NTf2−]. Both are conductors of DC electrical current, and their conductivity is modeled based on the electron-transfer self-exchange rate constants of their constituent redox-active species.

Mixed Linker Strategy for the Construction of a Fluorescent 2D Network Based on [Ag2(COO)2] as Secondary Building Unit

2013 ◽  
Vol 68 (4) ◽  
pp. 357-361 ◽  
Author(s):  
Di Sun ◽  
Shuai Yuan ◽  
Shan-Shan Liu ◽  
Ya-Qin Zhao ◽  
Lu-Lu Han ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Hydrogen Bonds ◽  
Room Temperature ◽  
Tetrahedral Coordination ◽  
Secondary Building Unit ◽  
Ultrasound Assisted ◽  
A Chain ◽  
2D Network ◽  
Distorted Tetrahedral Coordination

The ultrasound-assisted reaction of AgNO3, 2-amino-4,6-dimethylpyrimidine (dmapym) and 2,6-naphthalenedicarboxylic acid (H2npd) gave rise to a new 2D network of the formula [Ag2(dmapym)2(npd)]n (1). The atoms Ag1 and Ag2 in the complex show seesaw and distorted tetrahedral coordination geometries, respectively. The dmapym ligand acts as a bidentate bridge to bind paired Ag(I) ions into a chain. The chains are further connected by npd linkers to form the resultant 2D network reinforced by N-H···O hydrogen bonds between dmapym and npd. Weak C-H···p interactions are also found in the crystal structure. Complex 1 exhibits photoluminescence in the solid state at room temperature with an emission maximum at 418 nm upon excitation at 330 nm.

Conducting neutral gold bisdithiolene complex [Au(dspdt)2]˙

2020 ◽  
Vol 49 (39) ◽  
pp. 13737-13743
Author(s):  
Mariana F. G. Velho ◽  
Rafaela A. L. Silva ◽  
Graça Brotas ◽  
Elsa B. Lopes ◽  
Isabel C. Santos ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electrical Conductivity ◽  
Room Temperature ◽  
High Electrical Conductivity

A gold bisdithiolene complex with a unique crystal structure displays high electrical conductivity at room temperature.

FT-IR Micro-Spectroscopic Studies of Several Charge-Transfer Organic Electrical Conductors

1987 ◽  
Vol 41 (8) ◽  
pp. 1377-1382 ◽  
Author(s):  
John R. Ferraro ◽  
Hau H. Wang ◽  
John Ryan ◽  
Jack M. Williams
Keyword(s):  
Hydrogen Bonding ◽  
Charge Transfer ◽  
Room Temperature ◽  
Spectroscopic Studies ◽  
Infrared Reflectance ◽  
Bending Vibration ◽  
Ft Ir ◽  
Electrical Conductors ◽  
Reflectance Measurements ◽  
Vibrational Feature

A series of infrared reflectance measurements using FT-IR Micro methods were conducted on bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF or “ET”) and bis(propylenedithio)tetrathiafulvalene (BPDT or “PT”) salts of the type (ET)2 X, where X = I3, AuCl2−, AuBr2−, AuI2−, I2Br−, IBr2, ICl2, ReO4−, ClO4−, and [Formula: see text]; and (PT)2 X, where X = I3−, IBr2−, I2Br−, and ICl2−. The technique is useful for characterizing, at room temperature, differences between β-, β′- and α′-type structures vs. α-structures. The β-, β′-, and α′-type structures show a vibrational feature at ∼1280 cm−1 which has been assigned as the -C-C-H bending vibration and is absent in the spectrum of the α-type salts. This vibration shifts toward higher frequency in going from the PT to the ET salts, and the results indicate stronger hydrogen bonding and harder lattices in the ET salts as opposed to the PT salts. This frequency shift also appears to be a function of the electronegativity of the halogen in the anion moiety of the charge-transfer salt.

A Study of Substitution the Element of (La+3) on the Structural and Electrical Properties of the Compound Ferrite (𝐂𝐨𝟎.𝟐𝟓𝑵𝒊𝟎.𝟐𝟓𝐙𝐧𝟎.𝟓𝐋𝐚𝐱𝐅𝐞𝟐−𝐱𝐎𝟒)

2021 ◽  
Vol 19 (3) ◽  
pp. 56-61
Author(s):  
Bilal Ahmed Omar ◽  
Rabab Shakour Ali
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Electrical Conductivity ◽  
Electrical Properties ◽  
Spontaneous Combustion ◽  
Chemical Formula ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structural And Electrical Properties ◽  
Scanning Electron

The ferritic nanocomposite which prepared has the chemical formula of (Co0.25𝑁𝑖0.25Zn0.5LaxFe2−xO4), for different values of (X= 0, 0. 25, 0. 5, 0. 75), by using the spontaneous combustion-gel method, where calcination had been at temperature of (700˚C) for two hours; then studied the structural properties of the resulting ferrite via X-Ray diffraction (XRD), and Scanning Electron Microscopy (SEM) The results denote that the ferrite has a unique phase with a spinal-shaped crystal structure and a granular size are (23-36) nm, with increase in lattice constant of decrease in porosity, and electrical properties were also take in to consideration, like value of dielectric constant, the loss coefficient also observed via increase the frequency. The alternating electrical conductivity (σa.c) increases with increasing frequency.

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