scholarly journals Syntheses, Crystal Structures, and Properties of Six Coordination Complexes Based on a Newly Designed Mercapto-thiadiazole Ligand

2014 ◽  
Vol 67 (2) ◽  
pp. 241 ◽  
Author(s):  
Lu-Lu Wei ◽  
Lin-Ke Li ◽  
Li-Yan Fan ◽  
Chang-Hong Wang ◽  
Hong-Wei Hou
Keyword(s):  
Self Assembly ◽  
Free Ligand ◽  
Luminescent Properties ◽  
Coordination Complexes ◽  
Helical Chain ◽  
Thermal Stabilities ◽  
1D Chain ◽  
Photoactive Materials ◽  
3D Framework ◽  
Mononuclear Structure

Six coordination complexes were solvothermally synthesised: a 3D framework [Cd(tmtt)2]n (1), 2D architectures [Zn(tmtt)2]n (2) and [Pb(tmtt)2]n (3), 1D chain structures [Ni(tmtt)2·(H2O)2]n (4) and [Co(tmtt)2·(H2O)2]n (5), and a mononuclear structure [Hg(tmtt)2] (6). The complexes, based on self-assembly of different metal ions with a newly designed mercapto-thiadiazole ligand tmttH (tmttH = 5-[(1H-1,2,4-triazol-1-yl)methyl]-1,3,4-thiadiazole-2(3H)-thione), were characterised by single crystal X-ray diffraction analyses. Crystal structure analyses reveal that complex 1 exhibits a four-fold interpenetrating 3D framework with {64.82} topology based on two kinds of right-handed single-helical chains, 2 displays a bilayer structure, 3 presents a crown-shaped network, 4 and 5 show 1D double–helical chain structures, and 6 is a mononuclear structure. Moreover, the thermal stabilities of crystalline samples 1–6 have been investigated, and the luminescent properties of complexes 1, 2, 3, 6, and the free ligand have been studied. The results of photoluminescent measurements illustrate that 2 and 3 may serve as excellent candidates for potential photoactive materials.

Hydrothermal Syntheses, Crystal Structures, and Luminescent Properties of Two MnII Coordination Polymers: From Two-Fold Interpenetrated pcu Topological Net to Polycatenated 2D+2D→3D Framework

2015 ◽  
Vol 68 (2) ◽  
pp. 322 ◽  
Author(s):  
Wenlong Liu ◽  
Mengqiang Wu ◽  
Xueying Wang ◽  
Wei Wang ◽  
Dayu Liu ◽  
...  
Keyword(s):  
Dicarboxylic Acid ◽  
Coordination Polymers ◽  
Self Assembly ◽  
Room Temperature ◽  
Luminescent Properties ◽  
The Self ◽  
X Ray Diffraction ◽  
X Ray ◽  
3D Framework ◽  
Dimethyl Benzene

Using a hydrothermal synthesis, the self-assembly of MnII ions and 1,4-bis(1-imidazol-yl)-2,5-dimethyl benzene with two dicarboxylate ligands, 2-nitrobenzene-1,4-dicarboxylic acid (2-H2ata) and 5-methylbenzene-1,3-dicarboxylic acid (5-CH3-H2ip) constructed two interesting coordination polymers: [Mn(2-ata)(bimb)]n (1) and {[Mn(5-CH3-ip)(bimb)1.5]·2H2O}n (2), where bimb refers to 1,4-bis(1-imidazol-yl)-2,5-dimethyl benzene. Their structures were determined by single-crystal X-ray diffraction, elemental analysis, and infrared spectroscopy. Complex 1 exhibits a 2-fold interpenetrated pcu net. Complex 2 shows an unusual polycatenated 2D+2D→3D framework. In addition, the solid-state photoluminescent properties of 1 and 2 were investigated at room temperature.

scholarly journals Effect of Charge on the Structures of Zn(II) Coordination Polymers with Triazole-carboxylate Ligands: Syntheses, Structures, and Luminescent Properties

Crystals ◽  
2018 ◽  
Vol 8 (8) ◽  
pp. 312 ◽  
Author(s):  
Shaobin Miao ◽  
Xiaojuan Sun ◽  
Kexin Wang ◽  
Chunying Xu ◽  
Zhaohao Li ◽  
...  
Keyword(s):  
Coordination Polymers ◽  
Positive Charge ◽  
Luminescent Properties ◽  
Chain Structure ◽  
Double Layers ◽  
Carboxylate Ligands ◽  
Benzenedicarboxylic Acid ◽  
1D Chain ◽  
3D Framework ◽  
State Luminescence

Three new Zn(II) coordination polymers, {[Zn(L1)2(H2O)2]·4H2O}n (1), {[Zn(L2)(H2O)2]·0.5H2O}n (2), and {[Zn1.5(L1)(o-bdc)(H2O)]·0.5H2O}n (3) (HL1 = 3,5-di(1,2,4-triazol-1-yl)benzoic acid, H2L2 = 5-(triazol-1-yl)isophthalic acid, o-H2bdc = 1,2-benzenedicarboxylic acid), were successfully synthesized and characterized. Compound 1 exhibits 1D chain structure containing [Zn(L1)2] unit. Compound 2 shows a 2D plane with the ratio of Zn:L2 was 1:1 since L2 can match the positive charge of Zn(II). When L1 and o-bdc2– were presented together, Zn(II) centers are linked by L1 to form 2D double layers, then o-bdc2– further connected the adjacent layers to generate final 3D framework of 3. The ligand charges may play key roles in tuning the frameworks of compounds 1–3. The solid state luminescence of compounds 1–3 and all ligands have been investigated here.

Urothermal Syntheses, Crystal Structures, and Luminescent Properties of Two New ZnII Compounds Constructed by the Mixed Ligands of 1,2,4-Triazole and 1,4-Naphthalenedicarboxylic Acid or 2,6-Naphthalenedicarboxylic Acid

2015 ◽  
Vol 68 (8) ◽  
pp. 1299 ◽  
Author(s):  
Haiyan Liu ◽  
Xufeng Meng ◽  
Lihui Zhang ◽  
Anqiang Jia
Keyword(s):  
Self Assembly ◽  
Metal Organic Frameworks ◽  
Luminescent Properties ◽  
The Self ◽  
X Ray Diffraction ◽  
Thermal Stabilities ◽  
X Ray ◽  
Mixed Ligands ◽  
Elemental Analyses ◽  
Metal Organic

Under urothermal conditions, the self-assembly of ZnII ions, 1,2,3-triazole, and two isomeric dicarboxylate ligands (1,4-H2ndc and 2,6-H2ndc) afforded two new metal–organic frameworks, namely [Zn(1,4-ndc)0.5(taz)]n·n(e-urea) (1) and [Zn(2,6-ndc)0.5(taz)]n·n(H2O)·n(e-urea) (2) (1,4-H2ndc = 1,4-naphthalenedicarboxylic acid; 2,6-H2ndc = 2,6-naphthalenedicarboxylic acid; Htaz = 1,2,4-triazole; e-urea = ethyleneurea), which were further determined by single-crystal X-ray diffraction analyses, elemental analyses, powder X-ray diffraction analyses, and IR spectra. Compound 1 features a 3D pillar-layered framework with 6-connected pcu topology (pcu = α-Po), and compound 2 also features a 3D pillar-layered framework with 6-connected pcu topology. In addition, the thermal stabilities and solid-state photoluminescent properties of compounds 1 and 2 were also studied.

MAGNETIC NANOCHAINS: A REVIEW

NANO ◽  
2011 ◽  
Vol 06 (01) ◽  
pp. 1-17 ◽  
Author(s):  
HUI WANG ◽  
YIFEI YU ◽  
YUBIN SUN ◽  
QIANWANG CHEN
Keyword(s):  
Magnetic Field ◽  
Self Assembly ◽  
Magnetic Interactions ◽  
Synthesis Methods ◽  
Zero Field ◽  
Magnetic Recording Media ◽  
1D Chain ◽  
Potential Applications ◽  
Micromechanical Sensors ◽  
Nanoparticle Chains

One-dimensional (1D) chain-like structures are of special significance because of their interparticle magnetic interactions and potential applications in various fields, such as micromechanical sensors. This paper attempts to review the field of research into magnetic chains including monatomic chains and nanoparticle chains. The synthesis methods used mostly belong to one of the following categories: magnetosome chains in magnetotactic bacteria, zero-field self-assembly, magnetic field induced (MFI) assembly, template-directed synthesis, and gas phase synthesis. The potential applications of nanoparticle chains, mainly in the field of magnetic recording media, sensor, biomedicine and magnetic-field tunable photonic crystal are discussed.

scholarly journals Tuning Gel State Properties of Supramolecular Gels by Functional Group Modification

Molecules ◽  
2019 ◽  
Vol 24 (19) ◽  
pp. 3472 ◽  
Author(s):  
Dipankar Ghosh ◽  
Matthew T. Mulvee ◽  
Krishna K. Damodaran
Keyword(s):  
Self Assembly ◽  
Thermal Stabilities ◽  
Factors Affecting ◽  
Sem Image ◽  
Group Modification ◽  
Fibrous Morphology ◽  
Low Molecular Weight Gelators ◽  
Functional Group Modification ◽  
Gel Network ◽  
Weak Gels

The factors affecting the self-assembly process in low molecular weight gelators (LMWGs) were investigated by tuning the gelation properties of a well-known gelator N-(4-pyridyl)isonicotinamide (4PINA). The N―H∙∙∙N interactions responsible for gel formation in 4PINA were disrupted by altering the functional groups of 4PINA, which was achieved by modifying pyridyl moieties of the gelator to pyridyl N-oxides. We synthesized two mono-N-oxides (INO and PNO) and a di-N-oxide (diNO) and the gelation studies revealed selective gelation of diNO in water, but the two mono-N-oxides formed crystals. The mechanical strength and thermal stabilities of the gelators were evaluated by rheology and transition temperature (Tgel) experiments, respectively, and the analysis of the gel strength indicated that diNO formed weak gels compared to 4PINA. The SEM image of diNO xerogels showed fibrous microcrystalline networks compared to the efficient fibrous morphology in 4PINA. Single-crystal X-ray analysis of diNO gelator revealed that a hydrogen-bonded dimer interacts with adjacent dimers via C―H∙∙∙O interactions. The non-gelator with similar dimers interacted via C―H∙∙∙N interaction, which indicates the importance of specific non-bonding interactions in the formation of the gel network. The solvated forms of mono-N-oxides support the fact that these compounds prefer crystalline state rather than gelation due to the increased hydrophilic interactions. The reduced gelation ability (minimum gel concentration (MGC)) and thermal strength of diNO may be attributed to the weak intermolecular C―H∙∙∙O interaction compared to the strong and unidirectional N―H∙∙∙N interactions in 4PINA.

scholarly journals Synthesis, Crystal Structures and Luminescence Properties of Three New Cadmium 3D Coordination Polymers

Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2465
Author(s):  
Hai-Yan Ju ◽  
Gang Zhang ◽  
Ming Yang ◽  
De-Zheng Liu ◽  
Yong-Sheng Yang ◽  
...  
Keyword(s):  
Room Temperature ◽  
Coordination Complexes ◽  
Luminescence Properties ◽  
Solvothermal Reaction ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Π Stacking Interaction ◽  
2D Network ◽  
3D Framework

The new rigid planar ligand 2,5-bis(3-(pyridine-4-yl)phenyl)thiazolo[5,4-d]thiazole (BPPT) has been synthesized, which is an excellent building block for assembling coordination polymer. Under solvothermal reaction conditions, cadmium ion with BPPT in the presence of various carboxylic acids including (1,1′-biphenyl)-4,4′-dicarboxylic acid (BPDC), isophthalic acid (IP), and benzene-1,3,5-tricarboxylic acid (BTC) gave rise to three coordination complexes, viz, [Cd(BPPT)(BPDA)](BPPT)n (1), [Cd(BPPT) (IP)] (CH3OH) (2), and [Cd3(BPPT)3(BTC)2(H2O)2] (3). The structures of 1, 2, and 3 were characterized by single crystal X-ray diffraction. The IR spectra as well as thermogravimetric and luminescence properties were also investigated. Complex 1 is a two-dimensional (2D) network and further stretched to a 3D supramolecular structure through π–π stacking interaction. The complexes 2 and 3 show 3D framework. The complexes 1, 2, and 3 exhibited luminescence property at room temperature.

Substituent effects of two isophthalate derivatives on the construction of cadmium coordination polymers incorporating a dipyridyl ligand

2018 ◽  
Vol 74 (8) ◽  
pp. 894-900 ◽  
Author(s):  
Lin Wang ◽  
Qian-Kun Zhou ◽  
Yun Xu ◽  
Ni-Ya Li
Keyword(s):  
Coordination Polymers ◽  
Self Assembly ◽  
Three Dimensional ◽  
Substituent Effects ◽  
Dicarboxylic Acids ◽  
Two Dimensional ◽  
Reaction Conditions ◽  
Thermal Stabilities ◽  
Coordination Network ◽  
Potential Applications

In recent years, the design and construction of crystalline coordination complexes by the assembly of metal ions with multitopic ligands have attracted considerable attention because of the unique architectures and potential applications of these compounds. Two new coordination polymers, namely poly[[μ-trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene-κ2 N:N′](μ3-5-methylisophthalato-κ4 O 1,O 1′:O 3:O 3′)cadmium(II)], [Cd(C9H6O4)(C12H11N3)] n or [Cd(5-Me-ip)(2-NH2-3,4-bpe)] n , (I), and poly[[μ-trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene-κ2 N:N′](μ2-5-hydroxyisophthalato-κ4 O 1,O 1′:O 3:O 5)cadmium(II)], [Cd(C8H4O5)(C12H11N3)] n or [Cd(5-HO-ip)(2-NH2-3,4-bpe)] n , (II), have been prepared hydrothermally by the self-assembly of Cd(NO3)2·4H2O and trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene (2-NH2-3,4-bpe) with two similar dicarboxylic acids, i.e. 5-methylisophthalic acid (5-Me-H2ip) and 5-hydroxyisophthalic acid (5-HO-H2ip). The coordination network of (I) is a two-dimensional sql net parallel to (101). Adjacent sql nets are further linked to form a three-dimensional supramolecular framework via hydrogen-bonding interactions. Compound (II) is a two-dimensional (3,5)-connected coordination network parallel to (010) with the point symbol (63)(55647). As the other reactants and reaction conditions are the same, the structural differences between (I) and (II) are undoubtedly determined by the different substituent groups in the 5-position of isophthalic acid. Both (I) and (II) exhibit good thermal stabilities and photoluminescence properties.

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