Pb3Ba3Zn6(BO3)8 and α-BaZn2(BO3)2: new members of the zincoborates containing two different dimensional Zn–O units

2020 ◽  
Vol 7 (1) ◽  
pp. 101-107
Author(s):  
Xiaobo Pan ◽  
Hongping Wu ◽  
Shichao Cheng ◽  
Zhengping Wang
Keyword(s):  
High Temperature ◽  
Single Crystal ◽  
Solution Method ◽  
High Temperature Solution ◽  
X Ray Diffraction ◽  
New Members ◽  
X Ray ◽  
Temperature Solution ◽  
First Time

Two new zincoborates, namely, Pb3Ba3Zn6(BO3)8 and α-BaZn2(BO3)2, were synthesized by the high-temperature solution method and their structures were determined by single-crystal X-ray diffraction for the first time.

Synthesis and characterization of three new rare-earth orthoborates: Ba2MgY2(BO3)4, Ba2CdY2(BO3)4, and Ba2CdSc(BO3)3

2020 ◽  
Vol 49 (31) ◽  
pp. 10874-10879
Author(s):  
Runqing Liu ◽  
Hongping Wu ◽  
Hongwei Yu ◽  
Zhanggui Hu ◽  
Jiyang Wang ◽  
...  
Keyword(s):  
Rare Earth ◽  
High Temperature ◽  
Solution Method ◽  
Synthesis And Characterization ◽  
High Temperature Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Solution ◽  
First Time

Three rare-earth orthoborates Ba2MgY2(BO3)4, Ba2CdY2(BO3)4, and Ba2CdSc(BO3)3 were synthesized via a high-temperature solution method and their structures were determined by single crystal X-ray diffraction for the first time.

Effect of the cation size on the framework structures of magnesium tungstate, A4Mg(WO4)3 (A = Na, K), R2Mg2(WO4)3 (R = Rb, Cs)

2015 ◽  
Vol 44 (12) ◽  
pp. 5810-5817 ◽  
Author(s):  
Shujuan Han ◽  
Ying Wang ◽  
Qun Jing ◽  
Hongping Wu ◽  
Shilie Pan ◽  
...  
Keyword(s):  
High Temperature ◽  
Alkali Metal ◽  
Single Crystal ◽  
High Temperature Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Solution ◽  
Cation Size

A series of alkali metal magnesium tungstates, A4Mg(WO4)3 (A = Na, K), R2Mg2(WO4)3 (R = Rb, Cs), were synthesized from a high temperature solution, and their structures were determined by single-crystal X-ray diffraction.

Synthesis, crystal structure and luminescence properties of a new samarium borate phosphate, CsNa2Sm2(BO3)(PO4)2

2020 ◽  
Vol 76 (12) ◽  
pp. 1068-1075
Author(s):  
Dan Zhao ◽  
Lin-Ying Shi ◽  
Rui-Juan Zhang ◽  
Ya-Li Xue
Keyword(s):  
Crystal Structure ◽  
High Temperature ◽  
Three Dimensional ◽  
High Temperature Solution ◽  
X Ray Diffraction ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
Temperature Solution ◽  
Light Excitation ◽  
Total Structure

A new caesium sodium samarium borate phosphate, CsNa2Sm2(BO3)(PO4)2, has been obtained successfully by the high-temperature solution growth (HTSG) method and single-crystal X-ray diffraction analysis reveals that it crystallizes in the orthorhombic space group Cmcm. The structure contains BO3, PO4, NaO7 and SmO7 polyhedra which are interconnected via corner- or edge-sharing O atoms to form a three-dimensional [Na2Sm2(BO3)(PO4)2]∞ network. This network delimits large cavities where large Cs+ cations reside to form the total structure. Under 402 nm light excitation, CsNa2Sm2(BO3)(PO4)2 exhibits three emission bands due to the 4f→4f transitions of Sm3+. Furthermore, we introduced Gd3+ into Sm3+ sites to optimize the Sm3+ concentration and improve the luminescence intensity. The optimal concentration is Gd/Sm = 98/2. The luminescent lifetime of a series of CsNa2Gd2(1–x)Sm2x (BO3)(PO4)2 phosphors shows a gradual degradation of lifetime from 2.196 to 0.872 ms for x = 0.01–0.10. The Commission Internationale de l'Eclairage (CIE) 1931 calculation reveals that CsNa2Gd1.96Sm0.04(BO3)(PO4)2 can emit orange light under 402 nm excitation.

Top-seeded solution growth and characterization of Raman crystal LiVMoO6

RSC Advances ◽  
2016 ◽  
Vol 6 (109) ◽  
pp. 107519-107524 ◽  
Author(s):  
Zheng Wang ◽  
Qian Wu ◽  
Min Zhu ◽  
Zeliang Gao ◽  
Xiangxin Tian ◽  
...  
Keyword(s):  
High Temperature ◽  
Single Crystal ◽  
Solution Growth ◽  
High Temperature Solution ◽  
Temperature Solution ◽  
Top Seeded Solution Growth ◽  
First Time

Single crystal LiVMoO6, with dimensions up to 20 mm × 15 mm × 12 mm, has been grown successfully for the first time from a high-temperature solution with MoO3 as a flux.

Sn14O11Br6: A promising birefringent material with [Sn14O11Br6] layer

2021 ◽  
Author(s):  
Zixiu Lu ◽  
Fangfang Zhang ◽  
Abudukadi Tudi ◽  
Zhihua Yang ◽  
Shilie Pan
Keyword(s):  
High Temperature ◽  
Closed System ◽  
Solution Method ◽  
Two Dimensional ◽  
High Temperature Solution ◽  
Temperature Solution ◽  
First Time

The tin(Ⅱ) oxybromide, Sn14O11Br6 (TOB), was synthesized successfully via the high-temperature solution method in a closed system for the first time. Its structure displays two-dimensional [Sn14O11Br6] layers constructed from highly...

scholarly journals Eightfold Electrophilic Methylation of Octacyanotungstate [W(CN)8]4−/3−: Preparation of Homoleptic, Eight-coordinate Methylisocyanide Complexes [W(CNMe)8]4+/5+

2021 ◽  
Author(s):  
Malte Sellin ◽  
Susanne Margot Rupf ◽  
Ulrich Abram ◽  
Moritz Malischewski
Keyword(s):  
Sulfur Dioxide ◽  
Single Crystal ◽  
Epr Spectroscopy ◽  
X Ray Diffraction ◽  
Liquid Sulfur ◽  
Methyl Fluoride ◽  
X Ray ◽  
First Time ◽  
Ir And Raman ◽  
Methyl Triflate

Homoleptic eight-fold coordinated methylisocyanide complexes of W(IV) and W(V) have been prepared for the first time. The reaction of [NBu4]4[W(CN)8] with methyl triflate MeOTf gives [W(CNMe)8][OTf]4. The even stronger methylating mixture of methyl fluoride MeF and arsenic pentafluoride AsF5 in liquid sulfur dioxide SO2 is able to fully alkylate both [NBu4]4[W(CN)8] and [NBu4]3[W(CN)8]. The paramagnetic octakis(methylisocyanide)- tungsten(V) [W(CNMe)8][AsF6]5 is thermally highly unstable above −30 °C. All compounds have been characterized via single-crystal X-ray diffraction, IR and Raman, as well as NMR or EPR spectroscopy<br>

Niobium-bearing arsenides and germanides from elemental mixtures not involving niobium: a new twist to an old problem in solid-state synthesis

2018 ◽  
Vol 74 (5) ◽  
pp. 623-627 ◽  
Author(s):  
Sviatoslav Baranets ◽  
Hua He ◽  
Svilen Bobev
Keyword(s):  
High Temperature ◽  
Solid State ◽  
Diffraction Data ◽  
Alkaline Earth ◽  
Alkaline Earth Metals ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Temperature Reactions ◽  
First Time ◽  
Synthetic Work

Three isostructural transition-metal arsenides and germanides, namely niobium nickel arsenide, Nb0.92(1)NiAs, niobium cobalt arsenide, NbCoAs, and niobium nickel germanide, NbNiGe, were obtained as inadvertent side products of high-temperature reactions in sealed niobium containers. In addition to reporting for the very first time the structures of the title compounds, refined from single-crystal X-ray diffraction data, this article also serves as a reminder that niobium containers may not be suitable for the synthesis of ternary arsenides and germanides by traditional high-temperature reactions. Synthetic work involving alkali or alkaline-earth metals, transition or early post-transition metals, and elements from groups 14 or 15 under such conditions may yield Nb-containing products, which at times could be the major products of such reactions.

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