Synthesis of surfactant-free SnS nanoplates in an aqueous solution

RSC Advances ◽  
2015 ◽  
Vol 5 (115) ◽  
pp. 94796-94801 ◽  
Author(s):  
Heeseung Yang ◽  
Chang-Eun Kim ◽  
Anupam Giri ◽  
Aloysius Soon ◽  
Unyong Jeong
Keyword(s):  
Crystal Structure ◽  
Aqueous Solution ◽  
Chemical Transformation ◽  
Environmentally Friendly ◽  
Synthetic Route ◽  
Aqueous Conditions

A synthetic route to produce surfactant-free SnS nanoplates with the Pbnm crystal structure is suggested. The process is quick and environmentally-friendly, accomplished under mild aqueous conditions by chemical transformation.

Synthesis of Highly Luminescent Glutathione-Capped CdTe-Mn/ZnS Quantum Dots

2013 ◽  
Vol 668 ◽  
pp. 691-695
Author(s):  
Ying Fan Liu ◽  
Wei Feng He ◽  
Guo Qing Wang ◽  
Shao Ming Fang ◽  
Yu An Sun
Keyword(s):  
Aqueous Solution ◽  
Quantum Dots ◽  
Environmentally Friendly ◽  
Core Shell ◽  
Sulfur Source ◽  
Synthetic Route ◽  
Reaction Conditions ◽  
Optimum Reaction ◽  
High Fluorescence

A green synthetic route is reported for quickly synthesis of highly luminescent CdTe-Mn/ZnS quantum dots (QDs) in aqueous solution. Glutathione (GSH) was used as capping reagent and thioacetamide (TAA) as sulfur source for growth of ZnS shell on the CdTe-Mn QDs. At the optimum reaction conditions, the results indicate that the GSH-capped CdTe-Mn/ZnS QDs exhibit high fluorescence QYs and the best QY is 58%. These GSH-capped core-shell QDs exhibit excellent colloidal and photostability. This method is simple and environmentally friendly.

scholarly journals Zn–Catalyzed Direct Synthesis of 3-Iodo-1,3-dienes from α-Allenols

2020 ◽  
Vol 3 (1) ◽  
pp. 113
Author(s):  
Mireia Toledano-Pinedo ◽  
Beatriz Peñín ◽  
Teresa Martínez del Campo ◽  
Pedro Almendros
Keyword(s):  
Direct Synthesis ◽  
Environmentally Friendly ◽  
Synthetic Route

We wish to report herein a new protocol that allows one to obtain 3-iodo-1,3-dienes through a sustainable process starting from α-allenols. In this new synthetic route, zinc (II) derivatives are used as metallic promoter, which are an inexpensive and environmentally friendly species.

Unusual π-π interactions directed by [{(C6H6)Ru}2W8O30(OH)2]6– hybrid anion

CrystEngComm ◽  
2021 ◽  
Author(s):  
Anna A Mukhacheva ◽  
Vladislav Komarov ◽  
Vasily Kokovkin ◽  
Alexander S. Novikov ◽  
Pavel A Abramov ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Aqueous Solution ◽  
Building Block ◽  
Π Interactions

The [{(C6H6)Ru}2W8O30(OH)2]6– hybrid (organometallic-POM) anion was used as a pH-tunable building block to create special conditions for realizing π-π interactions in the crystal structure. Changing pH of aqueous solution of...

A green synthetic route for the surface-passivation of carbon dots as an effective multifunctional fluorescent sensor for the recognition and detection of toxic metal ions from aqueous solution

2019 ◽  
Vol 11 (4) ◽  
pp. 490-506 ◽  
Author(s):  
K. Radhakrishnan ◽  
P. Panneerselvam ◽  
M. Marieeswaran
Keyword(s):  
Aqueous Solution ◽  
Quantum Dots ◽  
Carbon Dots ◽  
Surface Passivation ◽  
Fluorescent Sensor ◽  
Toxic Metal ◽  
Carbon Quantum Dots ◽  
Synthetic Route ◽  
One Pot ◽  
Hydrothermal Methods

In this work, a green synthetic route was used to create a number of surface passivated fluorescent carbon quantum dots, which are explored as promising sensing probes, via facile one-pot hydrothermal methods.

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.

A succinct access to ω-hydroxylated jasmonates via olefin metathesis

2017 ◽  
Vol 72 (7-8) ◽  
pp. 285-292 ◽  
Author(s):  
Guillermo H. Jimenez-Aleman ◽  
Selina Seçinti ◽  
Wilhelm Boland
Keyword(s):  
Abiotic Stress ◽  
Olefin Metathesis ◽  
Higher Plants ◽  
Environmentally Friendly ◽  
Signaling Molecules ◽  
Synthetic Route ◽  
Limited Availability ◽  
Cross Metathesis ◽  
Physiological Processes

AbstractIn higher plants, jasmonates are lipid-derived signaling molecules that control many physiological processes, including responses to abiotic stress, defenses against insects and pathogens, and development. Among jasmonates, ω-oxidized compounds form an important subfamily. The biological roles of these ω-modified derivatives are not fully understood, largely due to their limited availability. Herein, a brief (two-step), simple and efficient (>80% yield), versatile, gram-scalable, and environmentally friendly synthetic route to ω-oxidized jasmonates is described. The approach utilizes olefin cross-metathesis as the key step employing inexpensive, commercially available substrates and catalysts.

A new three-dimensional anionic cadmium(II) dicyanamide network

2014 ◽  
Vol 70 (11) ◽  
pp. 1054-1056 ◽  
Author(s):  
Qiang Li ◽  
Hui-Ting Wang
Keyword(s):  
Crystal Structure ◽  
Aqueous Solution ◽  
Unit Cell Volume ◽  
Three Dimensional ◽  
Building Blocks ◽  
The Other ◽  
Dimensional Structure ◽  
Cadmium Nitrate ◽  
Nitrate Tetrahydrate ◽  
Anionic Framework

A new cadmium dicyanamide complex, poly[tetramethylphosphonium [μ-chlorido-di-μ-dicyanamido-κ4N1:N5-cadmium(II)]], [(CH3)4P][Cd(NCNCN)2Cl], was synthesized by the reaction of tetramethylphosphonium chloride, cadmium nitrate tetrahydrate and sodium dicyanamide in aqueous solution. In the crystal structure, each CdIIatom is octahedrally coordinated by four terminal N atoms from four anionic dicyanamide (dca) ligands and by two chloride ligands. The dicyanamide ligands play two different roles in the building up of the structure; one role results in the formation of [Cd(dca)Cl]2building blocks, while the other links the building blocks into a three-dimensional structure. The anionic framework exhibits a solvent-accessible void of 673.8 Å3, amounting to 47.44% of the total unit-cell volume. The cavities in the network are occupied by pairs of tetramethylphosphonium cations.

scholarly journals Crystal structure of the new hybrid material bis(1,4-diazoniabicyclo[2.2.2]octane) di-μ-chlorido-bis[tetrachloridobismuthate(III)] dihydrate

2015 ◽  
Vol 71 (11) ◽  
pp. 1384-1387
Author(s):  
Marwen Chouri ◽  
Habib Boughzala
Keyword(s):  
Crystal Structure ◽  
Aqueous Solution ◽  
Hydrogen Bonds ◽  
Room Temperature ◽  
Molar Ratio ◽  
Water Molecules ◽  
Site Symmetry ◽  
Two Dimensional ◽  
Slow Evaporation ◽  
Solution Ph

The title compound bis(1,4-diazoniabicyclo[2.2.2]octane) di-μ-chlorido-bis[tetrachloridobismuthate(III)] dihydrate, (C6H14N2)2[Bi2Cl10]·2H2O, was obtained by slow evaporation at room temperature of a hydrochloric aqueous solution (pH = 1) containing bismuth(III) nitrate and 1,4-diazabicyclo[2.2.2]octane (DABCO) in a 1:2 molar ratio. The structure displays a two-dimensional arrangement parallel to (100) of isolated [Bi2Cl10]4−bioctahedra (site symmetry -1) separated by layers of organic 1,4-diazoniabicyclo[2.2.2]octane dications [(DABCOH2)2+] and water molecules. O—H...Cl, N—H...O and N—H...Cl hydrogen bonds lead to additional cohesion of the structure.

A 35-year-old mystery solved: a facile synthetic route and structural confirmation of tetrachlorobis(diethyl ether)tungsten(IV)

2021 ◽  
Vol 77 (4) ◽  
Author(s):  
Thomas E. Shaw ◽  
Alfred P. Sattelberger ◽  
Titel Jurca
Keyword(s):  
Crystal Structure ◽  
Diethyl Ether ◽  
Thermal Instability ◽  
Room Temperature ◽  
Surface Characteristics ◽  
Hirshfeld Surface ◽  
Asymmetric Unit ◽  
Synthetic Route ◽  
X Ray ◽  
Elemental Analyses

The true identity of the diethyl ether adduct of tungsten(IV) chloride, WCl4(Et2O) x , has been in doubt since 1985. Initially postulated as the bis-adduct, WCl4(Et2O)2, questions arose when elemental analyses were more in line with a mono-ether adduct, viz. WCl4(Et2O). It was proposed that this was due to the thermal instability of the bis-adduct. Here, we report the room-temperature X-ray crystal structure and Hirshfeld surface characteristics of trans-tetrachloridobis(diethyl ether)tungsten(IV), trans-WCl4(Et2O)2 or trans-[WCl4(C4H10O)2]. The compound crystallizes, with half of the molecule in the asymmetric unit, in the centrosymmetric space group P21/n. The W—O distance is 2.070 (2) Å, while the W—Cl distances are 2.3586 (10) and 2.3554 (10) Å.

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