Synthesis of Mono‐coordinate Iron(II)‐phen Complex via a Solid State Ligand Exchange Process from Iron(II) Oxalate Dihydrate at Room Temperature under Mechanical Stressing

2005 ◽  
Vol 35 (5) ◽  
pp. 355-358 ◽  
Author(s):  
Tadashi Ohshita ◽  
Katsumasa Hirose ◽  
Motoo Komai ◽  
Mamoru Senna
Keyword(s):  
Solid State ◽  
Ligand Exchange ◽  
Room Temperature ◽  
Exchange Process ◽  
Oxalate Dihydrate

scholarly journals Recent Research Progress in Surface Ligand Exchange of PbS Quantum Dots for Solar Cell Application

2020 ◽  
Vol 10 (3) ◽  
pp. 975 ◽  
Author(s):  
Hyung Ryul You ◽  
Jin Young Park ◽  
Duck Hoon Lee ◽  
Younghoon Kim ◽  
Jongmin Choi
Keyword(s):  
Quantum Dots ◽  
Solid State ◽  
Ligand Exchange ◽  
Exchange Process ◽  
Surface States ◽  
Solution Phase ◽  
Research Progress ◽  
Solar Cell Application ◽  
Exchange Processes ◽  
Particle Size And Shape

Colloidal quantum dots (CQDs) are considered as next-generation semiconductors owing to their tunable optical and electrical properties depending on their particle size and shape. The characteristics of CQDs are mainly governed by their surface chemistry, and the ligand exchange process plays a crucial role in determining their surface states. Worldwide studies toward the realization of high-quality quantum dots have led to advances in ligand exchange methods, and these procedures are usually carried out in either solid-state or solution-phase. In this article, we review recent advances in solid-state and solution-phase ligand exchange processes that enhance the performance and stability of lead sulfide (PbS) CQD solar cells, including infrared (IR) CQD photovoltaics.

Nuclear Magnetic Resonance Studies of Co(II) Complexes of Thiourea and Related Ligands

1971 ◽  
Vol 49 (20) ◽  
pp. 3315-3326 ◽  
Author(s):  
D. R. Eaton ◽  
K. Zaw
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Ligand Exchange ◽  
Room Temperature ◽  
Equilibrium Constants ◽  
Exchange Process ◽  
Relative Importance ◽  
Proton Resonances ◽  
Dissociation Entropy ◽  
Nuclear Magnetic

A number of tetrahedral Co(II) complexes of thiourea, N-methyl thiourea, and N, N′-dimethyl thiourea have been studied by nuclear magnetic resonance (n.m.r.). All the complexes are paramagnetic and the proton resonances show large isotropic shifts in acetone-d6 solutions. The origin of these shifts is discussed. Two sets of resonances are observed for each position and this is attributed to restricted rotation about the C—N bond. The barrier for this rotation is higher in the complexes than in the free ligands. For all complexes the exchange between free and coordinated ligand is fast at room temperature but slow below −80 °C. The complexes are dissociated to a greater or lesser extent in acetone solution and equilibrium constants and other thermodynamic data are reported for this dissociation. Entropy differences are more important than energy differences in determining the extent of dissociation. It has been demonstrated that both associative and dissociative mechanisms play a part in the ligand exchange process. The relative importance of the two mechanisms differs in the various complexes.

Improved Sol-Gel Materials for Efficient Solid State Dye Lasers

1993 ◽  
Vol 329 ◽  
Author(s):  
Michael Canva ◽  
Patrick Georges ◽  
Jean-Fran^ois Perelgritz ◽  
Alain Brun ◽  
Fréddric Chaput ◽  
...  
Keyword(s):  
Solid State ◽  
Physical Properties ◽  
Room Temperature ◽  
Sol Gel ◽  
Tunable Lasers ◽  
Optical Quality ◽  
Dye Lasers ◽  
Laser Dyes ◽  
Host Matrix ◽  
Host Matrices

AbstractPhotoresistant laser dyes were trapped in silica based xerogel host matrices to obtain solid state tunable lasers. For this purpose very dense xerogel samples with improved chemical and physical properties were prepared at room temperature by the sol-gel technology. The as-prepared materials were polished to obtain optical quality surfaces and were used as new lasing media.Lasing action of such different dyes as rhodamine, perylene and pyrromethene doping dense sol-gel matrices was demonstrated. Efficiencies of 30 % or lifetimes of more than 100,000 shots were achieved with different new ≤dye dopant/host matrix≥ couples. Their different performances are reviewed and discussed.

Imidazole Promoted Efficient Anomerization of β-D-Glucose Pentaacetate in Organic Solutions and Solid State

2019 ◽  
Author(s):  
Meifeng Wang ◽  
Liyin Zhang ◽  
Yiqun Li ◽  
Liuqun Gu
Keyword(s):  
Solid State ◽  
Organic Solvents ◽  
Room Temperature ◽  
Materials Design ◽  
The Future ◽  
Organic Solutions ◽  
Glucose Pentaacetate

<p></p>Anomerization of glycosides were rarely performed under basic condition due to lack of efficiency. Here an imidazole promoted anomerization of β-D-glucose pentaacetate was developed; and reaction could proceed in both organic solvents and solid state at room temperature. Although mechanism is not yet clear, this unprecedent mild anomerization in solid state may open a new promising way for stereoseletive anomerization of broad glucosides and materials design in the future..

Circular dichroism and infrared study of β-turn formation in repeat peptides of elastin

1987 ◽  
Vol 52 (5) ◽  
pp. 1356-1361
Author(s):  
S. Abdel Rahman ◽  
M. Elsafty ◽  
A. Hattaba
Keyword(s):  
Circular Dichroism ◽  
Solid State ◽  
Ir Spectra ◽  
Chain Length ◽  
Room Temperature ◽  
Infrared Study ◽  
Feature Characteristic ◽  
C 50 ◽  
The Stability ◽  
Circular Dichroïsm

The conformation of elastin-like peptides Boc-Ala-Pro-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Ala-Pro-Gly-Val-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Gly-Val-Ala-Pro-Gly-Val-Gly-Val-APEGM were examined in solution using circular dichroism at 30 °C, 50 °C, and 70 °C and in solid state by IR at room temperature. The studies show that the β-turn is a significant conformational feature for peptides under investigation in solution at 30 °C and 50 °C, but at 70 °C the tetra, hexa, and decapeptides show the CD feature characteristic of the β-structure while the dodecapeptide spectra show the presence of β-turn which indicates the stability of the β-turn at this chain length. The IR spectra show that in the solid state at room temperature all investigated peptides assume essentially a β-turn except the tetrapeptide which present evidence of antiparallel β-structure. The β-turn contribution in the IR spectra increases with the increase of the chain length of the peptide.

scholarly journals Preparation of Li3PS4–Li3PO4 Solid Electrolytes by Liquid-Phase Shaking for All-Solid-State Batteries

2021 ◽  
Vol 2 (1) ◽  
pp. 39-48
Author(s):  
Nguyen H. H. Phuc ◽  
Takaki Maeda ◽  
Tokoharu Yamamoto ◽  
Hiroyuki Muto ◽  
Atsunori Matsuda
Keyword(s):  
Solid Solution ◽  
Solid State ◽  
Liquid Phase ◽  
Room Temperature ◽  
Reaction Medium ◽  
Magic Angle Spinning ◽  
Resonance Spectroscopy ◽  
Synthesis Methods ◽  
Magic Angle ◽  
Angle Spinning

A solid solution of a 100Li3PS4·xLi3PO4 solid electrolyte was easily prepared by liquid-phase synthesis. Instead of the conventional solid-state synthesis methods, ethyl propionate was used as the reaction medium. The initial stage of the reaction among Li2S, P2S5 and Li3PO4 was proved by ultraviolet-visible spectroscopy. The powder X-ray diffraction (XRD) results showed that the solid solution was formed up to x = 6. At x = 20, XRD peaks of Li3PO4 were detected in the prepared sample after heat treatment at 170 °C. However, the samples obtained at room temperature showed no evidence of Li3PO4 remaining for x = 20. Solid phosphorus-31 magic angle spinning nuclear magnetic resonance spectroscopy results proved the formation of a POS33− unit in the sample with x = 6. Improvements of ionic conductivity at room temperature and activation energy were obtained with the formation of the solid solution. The sample with x = 6 exhibited a better stability against Li metal than that with x = 0. The all-solid-state half-cell employing the sample with x = 6 at the positive electrode exhibited a better charge–discharge capacity than that employing the sample with x = 0.

Free-standing electrochemically coated MoSx based 3D-printed nanocarbon electrode for solid-state supercapacitor application

Nanoscale ◽  
2021 ◽  
Author(s):  
Kalyan Ghosh ◽  
Martin Pumera
Keyword(s):  
Solid State ◽  
Transition Metal ◽  
Electrochemical Deposition ◽  
Room Temperature ◽  
Free Standing ◽  
Metal Chalcogenide ◽  
Supercapacitor Application ◽  
3D Printed

Room temperature electrochemical deposition of transition metal chalcogenide (MoSx) on 3D-printed nanocarbon fibers based electrodes for custom shaped solid-state supercapacitor.

Sign in / Sign up

Export Citation Format

Share Document