Syntheses and Characterizations of Three Organically Templated Zinc Phosphites with 12-Ring Channels

2017 ◽  
Vol 70 (3) ◽  
pp. 286
Author(s):  
Zhen-Zhen Bao ◽  
Song-De Han ◽  
Jin-Hua Li ◽  
Guo-Ming Wang ◽  
Zong-Hua Wang
Keyword(s):  
Infrared Spectroscopy ◽  
Thermogravimetric Analysis ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Three Dimensional ◽  
Membered Ring ◽  
X Ray Diffraction ◽  
Organic Amine ◽  
X Ray ◽  
Hydroxyethyl Piperazine

Three new zinc phosphites, [Hapy]2[Zn3(HPO3)4] (1; apy = 4-aminopyridine), [H2hepip][Zn3(HPO3)4]·(H2O)0.25 (2; hepip = N-(2-hydroxyethyl)piperazine), and [H2tmdab][Zn3(HPO3)4] (3; tmdab = N,N,N′,N′-tetramethyl-1,3-diaminobutane), have been synthesized and characterized by infrared spectroscopy, elemental analysis, thermogravimetric analysis, and powder and single-crystal X-ray diffraction. The frameworks of 1–3 are constructed from 4-connected ZnO4 tetrahedra and 3-connected HPO3 pseudo pyramids with distinct connection mode driven by different organic amine templates. There are 12-membered ring (12-MR) and 8-MR apertures in the (3,4)-connected three-dimensional architecture of 1–3. It is notable that helical chains are observed in the framework of compound 3.

Synthesis, Structure and Properties of Two-Dimensional Coordination Polymer Based on 3,5-di(benzimidazol-1-yl)pyridine

2020 ◽  
Vol 42 (2) ◽  
pp. 249-249
Author(s):  
Guo Jun Wu Guo Jun Wu
Keyword(s):  
Infrared Spectroscopy ◽  
Coordination Polymer ◽  
Single Crystal ◽  
Photocatalytic Degradation ◽  
Elemental Analysis ◽  
Solvothermal Reaction ◽  
Two Dimensional ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
X Ray

[Cu(L)(AIP)·1.5H2O]n (1) [L= 3,5-di(benzimidazol-1-yl)pyridine, H2AIP= 5-aminoisophthalic acid] was prepared by the solvothermal reaction, which was characterized by single-crystal X–ray diffraction, infrared spectroscopy, and elemental analysis. 1 exhibits an infinite two dimensional [Cu(AIP)]n sheet parallel to (0 1 1) crystal plane. Furthermore, complex 1 displays good photocatalytic degradation of methyl blue (MB).

A Three-Dimensional Silver(I) Framework Assembled from Nitrilotriacetate

2005 ◽  
Vol 58 (2) ◽  
pp. 115 ◽  
Author(s):  
Chun-Long Chen ◽  
Qian Zhang ◽  
Ji-Jun Jiang ◽  
Qin Wang ◽  
Cheng-Yong Su
Keyword(s):  
Crystal Structure ◽  
Ir Spectroscopy ◽  
Coordination Polymer ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Three Dimensional ◽  
Single Crystal Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Coordination Numbers

The reaction of AgCF3CO2 with nitrilotriacetate (NTA) yields the three-dimensional silver(i) coordination polymer {Ag3[N(CH2COO)3]}n 1 which was characterized by means of elemental analysis and IR spectroscopy as well as X-ray diffraction. The single crystal structure shows that the NTA3– anions act as unusual heptadentate 13-coordination agents and the silver(i) atoms exhibit various coordination numbers in the range 3–6.

An unprecedented Zr-containing polyoxometalate tetramer with mixed trilacunary/dilacunary Keggin-type polyoxotungstate units

2018 ◽  
Vol 74 (11) ◽  
pp. 1284-1288 ◽  
Author(s):  
Zhong Zhang ◽  
Yue-Lin Wang ◽  
Guo-Yu Yang
Keyword(s):  
Thermogravimetric Analysis ◽  
Ir Spectroscopy ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Energy Dispersive ◽  
X Ray Diffraction ◽  
Remarkable Feature ◽  
Space Group ◽  
X Ray ◽  
Keggin Type

A novel zirconium(IV)-substituted tetramer polyoxotungstate, H6K4Na16[Zr4(β-GeW10O38)2(A-α-PW9O34)2]·37H2O, was synthesized hydrothermally and characterized by IR spectroscopy, elemental analysis, thermogravimetric analysis, powder X-ray diffraction, energy-dispersive X-ray spectroscopy and single-crystal X-ray diffraction. The compound crystallizes in the monoclinic P2/n space group. The most remarkable feature is that the centrosymmetric Zr-based polyoxotungstate tetramer consists of dilacunary Keggin-type germanotungstate and trilacunary Keggin-type phosphotungstate units that are linked by ZrIV ions.

Highest Connectivity in a Purely Inorganic 3D Compound Based on Paradodecatungstate-B Clusters: Synthesis and Magnetic Properties

2009 ◽  
Vol 64 (7) ◽  
pp. 809-814 ◽  
Author(s):  
Chun-Jing Zhang ◽  
Hai-Jun Pang ◽  
Ya-Guang Chen
Keyword(s):  
Magnetic Properties ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Uv Spectroscopy ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Simulation Procedure ◽  
3D Framework ◽  
Ir And Uv Spectroscopy

A new paradodecatungstate-B compound, [{Co(H2O)4}4(H4W12O42)]·10H2O (1) of the polyoxometalate series has been synthesized and characterized by elemental analysis, IR and UV spectroscopy, TG analysis, and single-crystal X-ray diffraction. Compound 1 exhibits a unique 8- connected three-dimensional (3D) framework with a (42 · 820 · 126) topology. Moreover, 1 displays antiferromagnetic interactions in the 2 - 300 K temperature range, well reproduced by a simulation procedure.

scholarly journals Bis(N,N′-bis(2-hydroxyethyl)ethylenediamine)nickel(II) saccharinate: synthesis, characterization and crystal structure

2015 ◽  
Vol 34 (1) ◽  
pp. 101
Author(s):  
Alparslan Karadogan ◽  
Ahmet Karadag ◽  
Veysel T. Yilmaz
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Complex Cation ◽  
Three Dimensional ◽  
Title Complex ◽  
X Ray Diffraction ◽  
X Ray ◽  
Distorted Octahedral

A new nickel(II) saccharinate (sac) complex containing <em>N</em>,<em>N</em>′-bis(2-hydroxyethyl)ethylenediamine (bishydeten), [Ni(bishydeten)<sub>2</sub>](sac)<sub>2</sub>, has been synthesized and characterized by elemental analysis, FTIR and single crystal X-ray diffraction. The title complex consists of a [Ni(bishydeten)<sub>2</sub>]<sup>2+</sup> cation and two sac anions. In the complex cation, the nickel(II) ion is coordinated by two neutral bishydeten ligands, leading to a distorted octahedral NiN<sub>4</sub>O<sub>2</sub> coordination, while both sac anions remain outside the coordination sphere. In the crystal, the complex cations and sac anions are connected by an extensive network of N–H∙∙∙N, N–H∙∙∙O, O–H∙∙∙O and C–H∙∙∙O hydrogen bonds into a three-dimensional supramolecular lattice.

Syntheses, Structures and Properties of a New Zn(II) Complex Based on the 2-(Benzoimidazol-2-yl-methyl)-1Htetrazole Ligand

2012 ◽  
Vol 67 (12) ◽  
pp. 1319-1324 ◽  
Author(s):  
Bingtao Liu ◽  
Rui Wang ◽  
Guiyang Zhang ◽  
Yanan Ding ◽  
Xiangru Meng
Keyword(s):  
Thermogravimetric Analysis ◽  
Ir Spectra ◽  
Single Crystal ◽  
Network Structure ◽  
Van Der Waals ◽  
Membered Ring ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structures And Properties ◽  
2D Network

A new Zn(II) complex [Zn2(bimt)2(Ac)(OH)]n (1) has been synthesized by the reaction of the flexible ligand 2-(benzoimidazol-2-yl-methyl)-1H-tetrazole (Hbimt) with Zn(Ac)2 · 2H2O and characterized by single-crystal X-ray diffraction and IR spectra. In complex 1, Zn1 and Zn2 ions are connected by μ2-bridging acetate and hydroxide groups to form a 6-membered ring. The bimt units coordinate to Zn1 and Zn2 ions in a bidentate bridging mode with two nitrogen atoms from the same benzoimidazole ring and connect the 6-membered rings resulting in the formation of a 2D network structure. Adjacent layers are further packed to a threedimensional network through van der Waals bonds. A thermogravimetric analysis was carried out, and the photoluminescent behavior of the complex was investigated.

scholarly journals An investigation of polyhedral deformation in two mixed-metal diarsenates: SrZnAs2O7and BaCuAs2O7

2015 ◽  
Vol 71 (4) ◽  
pp. 330-337 ◽  
Author(s):  
Sabina Kovač ◽  
Ljiljana Karanović ◽  
Tamara Đorđević
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
General Formula ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Open Framework ◽  
Geometrical Characteristics ◽  
Barium Copper

Two isostructural diarsenates, SrZnAs2O7(strontium zinc diarsenate), (I), and BaCuAs2O7[barium copper(II) diarsenate], (II), have been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. The three-dimensional open-framework crystal structure consists of corner-sharingM2O5(M2 = Zn or Cu) square pyramids and diarsenate (As2O7) groups. Each As2O7group shares its five corners with five differentM2O5square pyramids. The resulting framework delimits two types of tunnels aligned parallel to the [010] and [100] directions where the large divalent nine-coordinatedM1 (M1 = Sr or Ba) cations are located. The geometrical characteristics of theM1O9,M2O5and As2O7groups of known isostructural diarsenates, adopting the general formulaM1IIM2IIAs2O7(M1II= Sr, Ba, Pb;M2II= Mg, Co, Cu, Zn) and crystallizing in the space groupP21/n, are presented and discussed.

scholarly journals Valorization of Byproducts of Hemp Multipurpose Crop: Short Non-Aligned Bast Fibers as a Source of Nanocellulose

Molecules ◽  
2021 ◽  
Vol 26 (16) ◽  
pp. 4723
Author(s):  
Sara Dalle Vacche ◽  
Vijayaletchumy Karunakaran ◽  
Alessia Patrucco ◽  
Marina Zoccola ◽  
Loreleï Douard ◽  
...  
Keyword(s):  
Infrared Spectroscopy ◽  
Thermogravimetric Analysis ◽  
Cannabis Sativa ◽  
Crystallinity Index ◽  
Residual Lignin ◽  
Chemical Pretreatment ◽  
X Ray Diffraction ◽  
X Ray ◽  
Bast Fibers ◽  
Seed Maturity

Nanocellulose was extracted from short bast fibers, from hemp (Cannabis sativa L.) plants harvested at seed maturity, non-retted, and mechanically decorticated in a defibering apparatus, giving non-aligned fibers. A chemical pretreatment with NaOH and HCl allowed the removal of most of the non-cellulosic components of the fibers. No bleaching was performed. The chemically pretreated fibers were then refined in a beater and treated with a cellulase enzyme, followed by mechanical defibrillation in an ultrafine friction grinder. The fibers were characterized by microscopy, infrared spectroscopy, thermogravimetric analysis and X-ray diffraction after each step of the process to understand the evolution of their morphology and composition. The obtained nanocellulose suspension was composed of short nanofibrils with widths of 5–12 nm, stacks of nanofibrils with widths of 20–200 nm, and some larger fibers. The crystallinity index was found to increase from 74% for the raw fibers to 80% for the nanocellulose. The nanocellulose retained a yellowish color, indicating the presence of some residual lignin. The properties of the nanopaper prepared with the hemp nanocellulose were similar to those of nanopapers prepared with wood pulp-derived rod-like nanofibrils.

Synthesis and Crystal Structure of the Flexible Ligand Coordination Polymer [Co3(bpd)5.5(NCS)6(NH3)]n⋅2H2O(bpd= 1,4-bis (4-pyridyl)-2,3-diaza-1,3-butadiene)

2013 ◽  
Vol 803 ◽  
pp. 80-84
Author(s):  
Yu Qi Liu ◽  
Yong Yang ◽  
Rui Yang ◽  
Xiao Jun Xu
Keyword(s):  
Crystal Structure ◽  
Infrared Spectroscopy ◽  
Coordination Polymer ◽  
Single Crystal ◽  
X Ray Diffraction ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
Elemental Analyses ◽  
Ligand Coordination ◽  
Point Symbol

A novel metalorganic coordination polymer, namely [Co3(bpd)5.5(NCS)6(NH3)]n2H2O (1) (bpd=1,4-bis (4-pyridyl)-2,3-diaza-1,3-butadiene), has been synthesized and characterized by elemental analyses, infrared spectroscopy, and single-crystal X-ray diffraction. Compound 1 presents 2D[3,4,-connected 3-nodal net with the point symbol (4268210)(4462)(8210). In addition, four identical 2D single nets is interlocked with each other in parallel, thus directly leading to the formation of a polycatenated layer (2D2D).

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