Oxygen and peroxide bridged uranyl(vi) dimers bearing tetradentate hybrid ligands: supramolecular self-assembly and generation pathway

2020 ◽  
Vol 7 (18) ◽  
pp. 3412-3423 ◽  
Author(s):  
Jun Liu ◽  
Xueyu Wang ◽  
Baihua Chen ◽  
Lina Lv ◽  
Qiang Li ◽  
...  
Keyword(s):  
Single Crystal ◽  
Self Assembly ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Hybrid Ligands

Crystals of U(vi) complexes with N,N,N′,N′-tetramethyl-2,2′-bipyridine-6,6′-dicarboxamide and N,N,N′,N′-tetramethyl-1,10-phenanthroline-2,9-dicarboxamide were obtained under variable reaction conditions, and the structures were determined by single-crystal X-ray diffraction.

Crystal structures of (S)- and (R,S)-2,2′-bipyridine-3,3′-dicarboxylic acid 1,1′-dioxides and of their barium salts: absolute configuration and molecular distortion enforced by supramolecular self-assembly

1997 ◽  
Vol 212 (3) ◽  
Author(s):  
P. Vojtíšek ◽  
I. Císařová ◽  
J. Podlaha ◽  
Z. Žák ◽  
S. Böhm ◽  
...  
Keyword(s):  
Single Crystal ◽  
Dicarboxylic Acid ◽  
Crystal Structures ◽  
Absolute Configuration ◽  
Self Assembly ◽  
Barium Salt ◽  
X Ray Diffraction ◽  
X Ray

AbstractCrystal structures of the title compounds were determined by single crystal X-ray diffraction. Absolute configuration of the barium salt of (+)-(

Synthesis of Novel 2-Alkoxy-5H-benzo[6,7]cyclohepta[1,2-b]pyridine-3-carbonitriles

2003 ◽  
Vol 58 (7) ◽  
pp. 698-703 ◽  
Author(s):  
Adel S. Girgis ◽  
I. S. Ahmed-Farag
Keyword(s):  
Single Crystal ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Independent Synthesis

Reaction of 6-arylmethylene-6,7,8,9-tetrahydro-5H-benzocyclo-hepten-5-ones (1) with malononitrile in the appropriate alcohol in the presence of sodium afforded the corresponding 2-alkoxy-4-aryl- 6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine-3-carbonitriles (2) and not their isomeric forms 2-alkoxy-4-aryl-6,7-dihydro-5H-benzo[3,4]-cyclohepta[1,2-c]pyridine-1-carbonitriles (3). The proposed structure was confirmed via independent synthesis of (2) through the reaction of 6,7,8,9- tetrahydro-5-benzocycloheptenone (4) with the appropriate ylidenemalononitriles 5 under the same reaction conditions. Single crystal X-ray diffraction proves the structures of 2a,b.

Synthesis, Structure and Properties of a Novel Metal-Organic Coordination Polymer, [Zn (NH3)2(BDC)]n

2013 ◽  
Vol 575-576 ◽  
pp. 30-36 ◽  
Author(s):  
Ning Ning Wu ◽  
Can Xiong Guo ◽  
Gui An Wu ◽  
Zhao Cai ◽  
Wan Hong He
Keyword(s):  
Coordination Polymer ◽  
Single Crystal ◽  
Diffraction Analysis ◽  
Self Assembly ◽  
Terephthalic Acid ◽  
Differential Scanning Calorimetric ◽  
X Ray Diffraction ◽  
X Ray ◽  
Acid Ligand ◽  
Metal Organic

A novel one-dimensional metal-organic coordination polymer, [Zn (NH3)2(BDC)]n (BDC=1,4-benzenedicaboxylate), has been synthesized by solvent evaporation method through self-assembly of Zn (II) salts with terephthalic acid ligand in ammonia aqueous solution. Single crystal X-ray diffraction analysis indicated that each Zn (II) was coordinated by two nitrogen donors from two NH3 and two oxygen counter donors from terephthalic acid ligand. The adjacent zigzag chains are arranged in a parallel fashion and linked by interchain hydrogen bonding interaction and π-π stacking interactions into higher-dimensional framework. The compound has also been characterized by CHN elemental analyses, Single crystal X-ray diffraction analysis, powder X-ray diffraction (PXRD) analysis, Fourier transform infrared (FT-IR) spectra, Thermalgravimetric-differential scanning calorimetric (TG-DSC) and Solid-state nuclear magnetic resonance (NMR), etc. Results showed that the framework of compound was stable at the temperature up to 246°C. The desolvated product [Zn (BDC)]n, which was obtained by removal of molecular NH3 from [Zn (NH3)2(BDC)]n, can be transferred to the different skeleton structures through coordinating different small hydrogen-bond-forming molecules.

scholarly journals Ligand and solvent effects in the formation and self-assembly of a metallosupramolecular cage

2017 ◽  
Vol 41 (3) ◽  
pp. 1179-1185 ◽  
Author(s):  
N. N. Adarsh ◽  
Amarnath Chakraborty ◽  
Màrius Tarrés ◽  
Surjendu Dey ◽  
Fernando Novio ◽  
...  
Keyword(s):  
Coordination Polymer ◽  
Single Crystal ◽  
Solvent Effects ◽  
Self Assembly ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray

A metallosupramolecular cage and a one-dimensional coordination polymer have been synthesized and structurally characterized by single crystal X-ray diffraction.

Sn94– Zintl Ions as Reactive Precursor for Neat Solids: Syntheses and Crystal Structures of Rb4[SnTe4], KxCs4–x[SnTe4], and KxCs10–x[Sn4Te12]

2009 ◽  
Vol 64 (11-12) ◽  
pp. 1319-1324 ◽  
Author(s):  
Jian-Qiang Wang ◽  
Viktor Hlukhyy ◽  
Thomas F. Fässler
Keyword(s):  
Single Crystal ◽  
Crystal Structures ◽  
X Ray Diffraction ◽  
Compound K ◽  
Reaction Conditions ◽  
Elemental Tellurium ◽  
X Ray ◽  
Zintl Ions ◽  
Tetrahedral Anion

The reactions of Zintl ions Sn94− formed in ethylenediamine solutions of K2Cs2Sn9 and Rb4Sn9 with elemental tellurium have been investigated. Addition of elemental tellurium to the filtrates of these solutions leads - depending on the reaction conditions - to four different products: Compounds K0.36(1)Cs3.64(1)[SnTe4] (1) and Rb4[SnTe4] (2) contain the tetrahedral anion [SnTe4]4−, and Cs4[Sn2Te7] (3) features the anion [Te2Sn(μ-Te)(μ-Te2)SnTe2]4−, whereas a novel Zintl anion [Sn4Te12]10− is present in compound K0.44(1)Cs9.56(1)[Sn4Te12] (4). Compounds 1, 2 and 4 have been structurally characterized by single-crystal X-ray diffraction

scholarly journals Different Polyoxometalate Structures Obtained from the Na11H[H(2-x)Bi2W20O70(HWO3)x]·46H2O(x=1.4).

2018 ◽  
Vol 1 (2) ◽  
pp. 93-100
Author(s):  
Suhair Atta
Keyword(s):  
Single Crystal ◽  
Self Assembly ◽  
Multiple Testing ◽  
X Ray Diffraction ◽  
Triclinic Space Group ◽  
X Ray ◽  
Space Groups ◽  
Cell Parameters ◽  
New Family ◽  
Ft Ir

In the supramolecular chemistry world, Polyoxometalates (POMs) are considered as a new family of inorganic molecular containers, construct itself by self-assembly reaction from very small units, to form a cluster with unique structural and properties. three structures reported in this paper - differ in their unit cell parameters and also differ from the well-known - as the result of reaction of the Na11H[H(2- x)Bi2W20O70(HWO3)x]·46H2O (x=1.4) with Ca ion at different pH conditions. These structures are [Ca(H2O)7]2[Na(H2O)2]2[HBi2W20O70(HWO3)].14H2O(1), H2[NH4]10[HBi2W20O70(HWO3)] (2), and [NH4]6[Na(H2O)4]2[Ca(H2O)4]2[W12O42].2H2O (3). The last one is bismuth-free and it is formed through reassembly of the precursor. Full structural characterization was made by multiple testing techniques such as single-crystal X-ray diffraction, UV-visible spectroscopy, FT-IR, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). The single-crystal X-ray diffraction results for the three compounds are as follows:(1), Triclinic, space group P-1, while (2) and (3) crystallize in monoclinic space groups C2/m and P21/n respectively.

Hydrothermal Syntheses and Crystal Structures of Two New Mixed-valence Vanadium Oxides [Ni(en)2(H2O)2][Ni(en)3]2[V16O38Cl] · 3(H2O) and (H3O)2V3O8

2010 ◽  
Vol 65 (12) ◽  
pp. 1451-1456 ◽  
Author(s):  
Xing Liu ◽  
Xian-Hong Yin ◽  
Feng Zhang
Keyword(s):  
Vanadium Oxide ◽  
Single Crystal ◽  
Interlayer Space ◽  
Mixed Valence ◽  
Vanadium Oxides ◽  
Cluster Anions ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Molar Ratios

Two vanadium oxides [Ni(en)2(H2O)2][Ni(en)3]2[V16O38Cl] ・3(H2O) (1) (en = ethylenediamine) and (H3O)2 V3O8 (2) were hydrothermally synthesized and characterized by single-crystal X-ray diffraction. 1 consists of [Ni(en)2(H2O)2]2+ and [Ni(en)3]2+ cations, discrete [V16O38Cl]6− cluster anions and H2O molecules, while 2 consists of anionic mixed-valent V5+/V4+ vanadium oxide layers constructed from pairs of corner-sharing VVO4 tetrahedra and VIVO5 square pyramids, with H3O+ cations occupying the interlayer space. Both 1 and 2 were synthesized under the same reaction conditions but with different V/Ni molar ratios, which shows that the reactant stoichiometry of the system plays a key role in the formation of different structures in the products.

Mangan(II)-Komplexe mit dem vierzähnigen Stickstoffliganden C12H22N6(L): Synthese von [MnX2L] (X = Cl, Br, I, NCS), Kristallstrukturen von [MnCl2L] und [MnBr2L] / Manganese(II) Complexes with the Tetradentate Nitrogen Ligand C12H22N6(L): Synthesis of [MnX2L] (Χ = Cl, Br, I, NCS), Crystal Structures of [MnCl2L] and [MnBr2L]

1989 ◽  
Vol 44 (6) ◽  
pp. 632-636 ◽  
Author(s):  
Peter Stolz ◽  
Wolfgang Saak ◽  
Henry Strasdeit ◽  
Siegfried Pohl
Keyword(s):  
Single Crystal ◽  
Diffraction Data ◽  
Tetradentate Ligand ◽  
Distorted Tetrahedron ◽  
X Ray Diffraction ◽  
Orthorhombic Space Group ◽  
Reaction Conditions ◽  
X Ray ◽  
Nitrogen Ligand ◽  
Bond Lengths

[MnCl2(C12H22N6)] (1) and [MnBr2(C12H22N6)] (2) are obtained from the reaction of MnX2 (X = Cl, Br) with C12H22N6 in methanolic solution.In chloroform MnI2, OPPh3, and C12H22N6 react to give [MnI2(C12H22N6)] (3). With small variations of the reaction conditions [MnI2(C12H22N6)] · xCHCl3 (4) may be crystallized. The reaction of [Mn(NCS)2(OPPh3)4] with C12H22N6 in CHCl3 solution gives [Mn(NCS)2(C12H22N6)] · xCHCl3 (5). The structures of 1 and 2 were determined from single crystal X-ray diffraction data. The isotypic compounds crystallize in the orthorhombic space group Pbcn with Z = 4; 1: a = 1592.4(1), b = 785.0(1), c = 1270.7(1) pm; 2: a = 1590.0(1), b = 802.6(1), c = 1316.6(1) pm. C12H22N6 acts as a tetradentate ligand. The isolated complexes exhibit a twofold symmetry.Manganese(II) is in a six-coordinate environment, which can be described better as a distorted tetrahedron with two additional Mn-N bonds rather than as a distorted octahedron.The Mn-N bond lengths are 229.9(1) and 248.7(1) pm for 1 and 228.2(3) and 248.4(3) pm for 2. The Mn-Hal bond lengths are 239.2(1) (1) and 254.2(1) pm (2)

Self-Assembling l-d-l-Tripeptides Dance the Twist

Synlett ◽  
2020 ◽  
Vol 31 (05) ◽  
pp. 434-438 ◽  
Author(s):  
Maria C. Cringoli ◽  
Ottavia Bellotto ◽  
Rita De Zorzi ◽  
Attilio V. Vargiu ◽  
Silvia Marchesan
Keyword(s):  
Molecular Dynamics ◽  
Amino Acids ◽  
Single Crystal ◽  
Self Assembly ◽  
Building Blocks ◽  
Supramolecular Structures ◽  
X Ray Diffraction ◽  
Supramolecular Materials ◽  
X Ray ◽  
Self Assembling

Minimalistic peptides composed of d- and l-amino acids are attractive building blocks for functional supramolecular materials, including catalysts. d-Amino acids have long been known to promote turn conformations in peptides, yet unexpected twists continue to emerge on their effects on self-assembly. The combination of single-crystal X-ray diffraction and full-atom molecular dynamics have finally unraveled fine details of how l-d-l-tripeptides visit different conformations in solution and establish key interactions in supramolecular structures.

scholarly journals Self-assembly of metallosupramolecular rhombi from chiral concave 9,9’-spirobifluorene-derived bis(pyridine) ligands

2014 ◽  
Vol 10 ◽  
pp. 432-441 ◽  
Author(s):  
Rainer Hovorka ◽  
Sophie Hytteballe ◽  
Torsten Piehler ◽  
Georg Meyer-Eppler ◽  
Filip Topić ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Nmr Spectroscopy ◽  
Single Crystal ◽  
Self Assembly ◽  
The Self ◽  
Assembly Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pyridine Ligands ◽  
Racemic Form

Two new 9,9’-spirobifluorene-based bis(4-pyridines) were synthesised in enantiopure and one also in racemic form. These ligands act as concave templates and form metallosupramolecular [(dppp)2M2L2] rhombi with cis-protected [(dppp)Pd]2+ and [(dppp)Pt]2+ ions. The self-assembly process of the racemic ligand preferably occurs in a narcissistic self-recognising manner. Hence, a mixture of all three possible stereoisomers [(dppp)2M2{(R)-L}2](OTf)4, [(dppp)2M2{(S)-L}2](OTf)4, and [(dppp)2M2{(R)-L}{(S)-L}](OTf)4 was obtained in an approximate 1.5:1.5:1 ratio which corresponds to an amplification of the homochiral assemblies by a factor of approximately three as evidenced by NMR spectroscopy and mass spectrometry. The racemic homochiral assemblies could also be characterised by single crystal X-ray diffraction.

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