The cation and anion bonding modes make the difference: an unprecedented layered structure and a tri(hetero)nuclear moiety in thioantimonates(V)

2021 ◽  
Author(s):  
Wolfgang Bensch ◽  
Tobias Engesser ◽  
Christian Nather ◽  
Dario Broich ◽  
Felix Danker
Keyword(s):  
Aqueous Solution ◽  
Layered Structure ◽  
Room Temperature ◽  
The Difference

Mixing solutions of M2+ (M = Cu2+ or Zn2+) salts containing cyclam (cyclam = 1,4,8,11-tetraazacyclotetradecane) as ligand and an aqueous solution of Na3SbS4·9H2O at room temperature afforded crystallization of two...

Characteristics of Helium Diffusion Trajectory: A Molecular Dynamics Study

2013 ◽  
Author(s):  
Min Chen
Keyword(s):  
Molecular Dynamics ◽  
Helium Atom ◽  
Layered Structure ◽  
Room Temperature ◽  
The Difference ◽  
Increasing Temperature ◽  
He Atom ◽  
Helium Diffusion

Molecular dynamics (MD) are employed to explore the features of Helium atom and He clusters diffusion in titanium at the temperatures between room temperature and 667k. The results demonstrate that the frequency for Helium atom jumping from site to site increases with the increasing temperature. Another important feature is that the diffusion of a He atom and a He trimer is a layered structure. The difference is that the trajectory of a He atom is between two Ti atom layers of (001) planes, and the trajectory of a He trimer is overlapped with the Ti atom layers of (001) plane. Meanwhile, it is observed that the layered structured diffusion becomes ambiguous for a He atom and a He trimer when the temperature is increased. The conclusion emphasizes different migration features for He clusters of various sizes.

scholarly journals Practical Synthesis of 2-Iodosobenzoic Acid (IBA) without Contamination by Hazardous 2-Iodoxybenzoic Acid (IBX) under Mild Conditions

Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1897
Author(s):  
Hideyasu China ◽  
Nami Kageyama ◽  
Hotaka Yatabe ◽  
Naoko Takenaga ◽  
Toshifumi Dohi
Keyword(s):  
Aqueous Solution ◽  
Room Temperature ◽  
Practical Method ◽  
Hypervalent Iodine ◽  
Mild Conditions ◽  
Sequential Procedures ◽  
Iodine Compounds ◽  
Practical Synthesis ◽  
Iodosobenzoic Acid ◽  
Lower Temperature

We report a convenient and practical method for the preparation of nonexplosive cyclic hypervalent iodine(III) oxidants as efficient organocatalysts and reagents for various reactions using Oxone® in aqueous solution under mild conditions at room temperature. The thus obtained 2-iodosobenzoic acids (IBAs) could be used as precursors of other cyclic organoiodine(III) derivatives by the solvolytic derivatization of the hydroxy group under mild conditions of 80 °C or lower temperature. These sequential procedures are highly reliable to selectively afford cyclic hypervalent iodine compounds in excellent yields without contamination by hazardous pentavalent iodine(III) compound.

scholarly journals Self-assembly induced luminescence of Eu3+-complexes and application in bioimaging

2021 ◽  
Author(s):  
Ping-Ru Su ◽  
Tao Wang ◽  
Pan-Pan Zhou ◽  
Xiao-Xi Yang ◽  
Xiao-Xia Feng ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Rare Earth ◽  
Luminescence Intensity ◽  
Self Assembly ◽  
Room Temperature ◽  
Molecular Motion ◽  
Proof Of Concept ◽  
Room Temperature Phosphorescence ◽  
New Strategy ◽  
Size Controlled

Abstract Design and engineering of highly efficient emitting materials with assembly-induced luminescence, such as room temperature phosphorescence (RTP) and aggregation-induced emission (AIE), have stimulated extensive efforts. Here, we propose a new strategy to obtain size-controlled Eu3+-complex nanoparticles (Eu-NPs) with self-assembly induced luminescence (SAIL) characteristics without encapsulation or hybridization. Compared with previous RTP or AIE materials, the SAIL phenomena of increased luminescence intensity and lifetime in aqueous solution for the proposed Eu-NPs are due to the combined effect of self-assembly in confining the molecular motion and shielding the water quenching. As a proof of concept, we also show that this system can be further applied in bioimaging, temperature measurement and HClO sensing. The SAIL activity of the rare-earth (RE) system proposed here offers a further step forward on the roadmap for the development of RE light conversion systems and their integration in bioimaging and therapy applications.

A new one-dimensional CdIIcoordination polymer with a two-dimensional layered structure incorporating 2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole and benzene-1,2-dicarboxylate ligands

2016 ◽  
Vol 72 (6) ◽  
pp. 480-484 ◽  
Author(s):  
Qiu-Ying Huang ◽  
Xiao-Yi Lin ◽  
Xiang-Ru Meng
Keyword(s):  
Layered Structure ◽  
Room Temperature ◽  
Weak Interactions ◽  
Coordination Geometry ◽  
Dimensional Chain ◽  
Two Dimensional ◽  
One Dimensional ◽  
Heterocyclic Ligand ◽  
Rich Variety ◽  
Solvent Molecules

The N-heterocyclic ligand 2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole (imb) has a rich variety of coordination modes and can lead to polymers with intriguing structures and interesting properties. In the coordination polymercatena-poly[[cadmium(II)-bis[μ-benzene-1,2-dicarboxylato-κ4O1,O1′:O2,O2′]-cadmium(II)-bis{μ-2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole}-κ2N2:N3;κ2N3:N2] dimethylformamide disolvate], {[Cd(C8H4O4)(C11H10N4)]·C3H7NO}n, (I), each CdIIion exhibits an irregular octahedral CdO4N2coordination geometry and is coordinated by four O atoms from two symmetry-related benzene-1,2-dicarboxylate (1,2-bdic2−) ligands and two N atoms from two symmetry-related imb ligands. Two CdIIions are connected by two benzene-1,2-dicarboxylate ligands to generate a binuclear [Cd2(1,2-bdic)2] unit. The binuclear units are further connected into a one-dimensional chain by pairs of bridging imb ligands. These one-dimensional chains are further connected through N—H...O hydrogen bonds and π–π interactions, leading to a two-dimensional layered structure. The dimethylformamide solvent molecules are organized in dimeric pairsviaweak interactions. In addition, the title polymer exhibits good fluorescence properties in the solid state at room temperature.

Notizen:Phosphorescence Decay in Thallium-Doped Ammonium Chloride

1978 ◽  
Vol 33 (10) ◽  
pp. 1241-1242 ◽  
Author(s):  
S. Chaudhari ◽  
T. R. Joshi ◽  
R. V. Joshi
Keyword(s):  
Aqueous Solution ◽  
Ammonium Chloride ◽  
Mechanical Treatment ◽  
Room Temperature ◽  
Host Lattice ◽  
Luminescence Decay ◽  
Decay Rates ◽  
Negative Ion ◽  
Ultraviolet Emission ◽  
Near Ultraviolet

Abstract The phosphorescence decay rates of thallium-doped ammonium chloride (NH4Cl:Tl) phosphors, prepared by crystallization from aqueous solution, have been studied at room temperature for near-ultraviolet emission. The effects of impurity concentration as well as thermal and/or mechanical treatment on the decay rates have been examined. Phosphorescence centres consisting of a Tl+ion and a nearby negative ion vacancy are suggested to be responsible for the observed luminescence decay. The changes in the decay characteristics after pretreatments are explained on the basis of the location of the centres in normal and distorted regions of the host lattice.

A facile room temperature chemical transformation approach for binder-free thin film formation of Ag2Te and lithiation/delithiation chemistry of the film

2016 ◽  
Vol 45 (43) ◽  
pp. 17312-17318 ◽  
Author(s):  
Eun-Kyung Kim ◽  
Dasom Park ◽  
Nabeen K. Shrestha ◽  
Jinho Chang ◽  
Cheol-Woo Yi ◽  
...  
Keyword(s):  
Thin Film ◽  
Thin Films ◽  
Aqueous Solution ◽  
Ion Exchange ◽  
Chemical Transformation ◽  
Room Temperature ◽  
Film Formation ◽  
Synthetic Method ◽  
Binder Free ◽  
Thin Film Formation

An aqueous solution based synthetic method for binder-free Ag2Te thin films using ion exchange induced chemical transformation of Ag/AgxO thin films.

Effects of Aging on the Solubility of Palladium

1995 ◽  
Vol 412 ◽  
Author(s):  
C. Oda ◽  
H. Yoshikawa ◽  
M. Yui
Keyword(s):  
Aqueous Solution ◽  
Aging Time ◽  
Room Temperature ◽  
High Level Waste ◽  
Anaerobic Conditions ◽  
Dilute Aqueous Solution ◽  
Waste Repository ◽  
Ph Range ◽  
Effects Of Aging ◽  
High Level

AbstractPalladium solubility was measured in a dilute aqueous solution at room temperature in the pH range from 3 to 13 under anaerobic conditions. Crystalline Pd metal was clearly visible and the concentration of palladium in solution decreased gradually with aging time. The palladium concentrations in solution were less than 9.4×10-10M in the pH range from 4 to 10 and increased to 10-7M in the pH range greater than 10. This study suggests that palladium concentrations in certain high-level waste repository environments may be limited by Pd metal and may be less than 10-9M.

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