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Full-Text Articles in Physical Sciences and Mathematics
Synthesis And Anti-Leukaemic Activity Of Pyrrolo[3,2,1-Hi]Indole-1,2- Diones, Pyrrolo[3,2,1-Ij]Quinoline-1,2-Diones And Other Polycyclic Isatin Derivatives, Lidia Matesic, Julie M. Locke, Kara Vine, Marie Ranson, John B. Bremner, Danielle Skropeta
Synthesis And Anti-Leukaemic Activity Of Pyrrolo[3,2,1-Hi]Indole-1,2- Diones, Pyrrolo[3,2,1-Ij]Quinoline-1,2-Diones And Other Polycyclic Isatin Derivatives, Lidia Matesic, Julie M. Locke, Kara Vine, Marie Ranson, John B. Bremner, Danielle Skropeta
Danielle Skropeta
To further expand the structure–cytotoxic activity relationships of isatin derivatives and to reduce flexibility in substituent groups at nitrogen, 20 analogues incorporating a ring system between the N1 and C7 atoms of isatin were prepared using a variety of synthetic strategies. This yielded pyrroloindole-, pyrroloquinoline-, pyrroloacridine-, pyrrolophenanthridine- and benzopyrrolophenanthridine-based systems with embedded isatin moieties, the latter possessing a novel carbon skeleton. These compounds were subsequently assessed for their in vitro cytotoxicity against human U937 lymphoma cells, with the brominated pyrroloacridine dione 27 showing the most promising activity (IC50 3.01 μM) after 24 h.
The First Syntheses Of Enantiopure 2,2 '-Biindoline, Steven M. Wales, Anthony C. Willis, Paul A. Keller
The First Syntheses Of Enantiopure 2,2 '-Biindoline, Steven M. Wales, Anthony C. Willis, Paul A. Keller
Paul Keller
The first two syntheses of chiral 2,2'-biindoline are reported either in five steps from 2,2'-bioxirane, or three steps from 2,2'-biaziridine, both with exceptional enantiopurity
Advanced Chemical Oxidation Of 2,4,6-Trichlorophenol By Using Fenton's Reagent - Dechlorination And Toxicity Reduction, Kuang-Wei (Stone) Chen, Irvine W. Wei
Advanced Chemical Oxidation Of 2,4,6-Trichlorophenol By Using Fenton's Reagent - Dechlorination And Toxicity Reduction, Kuang-Wei (Stone) Chen, Irvine W. Wei
Irvine W. Wei
Chlorinated phenols are priority pollutants, regulated by stringent discharge limits. The presence of chlorine increases the toxicity of these phenolic compounds and decreases their biodegradability. This study is to examine the removal of a priority chlorinated aromatic pollutant, 2,4,6-trichlorophenol (TCP), in aqueous solution by using Fenton's Reagent (a mixture of hydrogen peroxide and fenous iron catalyst), in terms of dechlorination and toxicity reduction. Test results indicate that the higher the molar ratio of H₂O₂ to TCP, the faster the release of chloride from TCP. However, the chloride released in all runs eventually approach the same level of theoretical chloride concentration, …
Concerted Ho2 Elimination From Alpha-Aminoalkylperoxyl Free Radicals: Experimental And Theoretical Evidence From The Gas-Phase Nh2 Chco2 - + O2 Reaction, Gabriel Da Silva, Benjamin Kirk, Celli Lloyd, Adam Trevitt, Stephen Blanksby
Concerted Ho2 Elimination From Alpha-Aminoalkylperoxyl Free Radicals: Experimental And Theoretical Evidence From The Gas-Phase Nh2 Chco2 - + O2 Reaction, Gabriel Da Silva, Benjamin Kirk, Celli Lloyd, Adam Trevitt, Stephen Blanksby
Adam Trevitt
We have investigated the gas-phase reaction of the α- aminoacetate (glycyl) radical anion (NH2 •CHCO2−) with O2 using ion trap mass spectrometry, quantum chemistry, and statistical reaction rate theory. This radical is found to undergo a remarkably rapid reaction with O2 to form the hydroperoxyl radical (HO2 •) and an even-electron imine (NHCHCO2−), with experiments and master equation simulations revealing that reaction proceeds at the ion−molecule collision rate. This reaction is facilitated by a low-energy concerted HO2 • elimination mechanism in the NH2CH(OO•)CO2− peroxyl radical. These findings can explain the widely observed free-radical-mediated oxidation of simple amino acids to amides …
Gas-Phase Reactions Of Aryl Radicals With 2-Butyne: An Experimental And Theoretical Investigation Employing The N-Methyl-Pyridinium-4-Yl Radical Cation, Adrian Lam, Cong Li, George Khairallah, Benjamin Kirk, Stephen Blanksby, Adam Trevitt, Uta Wille, Richard O'Hair, Gabriel Da Silva
Gas-Phase Reactions Of Aryl Radicals With 2-Butyne: An Experimental And Theoretical Investigation Employing The N-Methyl-Pyridinium-4-Yl Radical Cation, Adrian Lam, Cong Li, George Khairallah, Benjamin Kirk, Stephen Blanksby, Adam Trevitt, Uta Wille, Richard O'Hair, Gabriel Da Silva
Adam Trevitt
Aromatic radicals form in a variety of reacting gas-phase systems, where their molecular weight growth reactions with unsaturated hydrocarbons are of considerable importance. We have investigated the ion–molecule reaction of the aromatic distonic N-methyl-pyridinium-4-yl (NMP) radical cation with 2-butyne (CH3C≡CCH3) using ion trap mass spectrometry. Comparison is made to high-level ab initio energy surfaces for the reaction of NMP and for the neutral phenyl radical system. The NMP radical cation reacts rapidly with 2-butyne at ambient temperature, due to the apparent absence of any barrier. The activated vinyl radical adduct predominantly dissociates via loss of a H atom, with lesser …
Phase Gap In Pseudoternary R1-Yry Mn2x 2-Xxx Compounds, Jianli Wang, S J. Kennedy, S J. Campbell, M Hofmann, S X. Dou
Phase Gap In Pseudoternary R1-Yry Mn2x 2-Xxx Compounds, Jianli Wang, S J. Kennedy, S J. Campbell, M Hofmann, S X. Dou
Jianli Wang
Our neutron diffraction investigation of PrMn2Ge2−xSix reveals a clear separation into two magnetic phases, canted ferromagnetic (Fmc) and antiferromagnetic (AFmc), between x = 1.0 and 1.2 and a commensurate phase gap in the lattice, due to magnetostrictive distortion. This remarkable magnetoelastic phenomenon is driven by a nonuniform atomic distribution on the X site which in turn produces subtle variations in the local lattice and abrupt changes in the Mn-Mn magnetic exchange interaction. Our results show that coexistence of Fmc and AFmc phases depends on lattice parameter, chemical pressure from the rare-earth and metalloid sites, and local lattice strain distributions. We …
Infrared Spectra Of The Li +_(H 2)N(N=1-3) Cation Complexes, C Emmeluth, B L. J Poad, C D. Thompson, G H. Weddle, E J. Bieske
Infrared Spectra Of The Li +_(H 2)N(N=1-3) Cation Complexes, C Emmeluth, B L. J Poad, C D. Thompson, G H. Weddle, E J. Bieske
Berwyck L. J. Poad
The Li+–(H2)n n = 1–3 complexes are investigated through infrared spectra recorded in the H–H stretch region (3980–4120 cm−1) and through ab initio calculations at the MP2∕aug-cc-pVQZ level. The rotationally resolved H–H stretch band of Li+–H2 is centered at 4053.4 cm−1 [a −108 cm−1 shift from the Q1(0) transition of H2]. The spectrum exhibits rotational substructure consistent with the complex possessing a T-shaped equilibrium geometry, with the Li+ ion attached to a slightly perturbed H2 molecule. Around 100 rovibrational transitions belonging to parallel Ka = 0‐0, 1-1, 2-2, and 3-3 subbands are observed. The Ka = 0‐0 and 1-1 transitions …
Infrared Spectra Of Cl-_(C6h6)Mm=1, 2, Christopher Thompson, Berwyck Poad, Corinna Emmeluth, Evan Bieske
Infrared Spectra Of Cl-_(C6h6)Mm=1, 2, Christopher Thompson, Berwyck Poad, Corinna Emmeluth, Evan Bieske
Berwyck L. J. Poad
The Cl--(C6H6)Arn n = 0,1,2 and Cl--(C6H6)2 complexes are investigated using photodissociation infrared spectroscopy in the CH stretch region and through ab initio calculations at the MP2/aug-cc-pVDZ level. The results indicate that Cl--C6H6 possesses a planar structure in which the benzene molecule is attached to the Cl- anion by a double hydrogen bond. The calculations predict that Cl (C6H6)2 has a C2 symmetry structure in which the two face-to-face benzene molecules are attached to …
1,2,4-Triazine-Accelerated Azide-Alkyne Cycloaddition And Synthesis Of Metalloenzyme Inhibitors, Belinda Shea Lady
1,2,4-Triazine-Accelerated Azide-Alkyne Cycloaddition And Synthesis Of Metalloenzyme Inhibitors, Belinda Shea Lady
Doctoral Dissertations
The work of this dissertation describes the design and synthesis of 1,2,4-triazine ligands and other N-containing heterocycles and their use in the copper-catalyzed azide-alkyne cycloaddition (CuAAC). A variety of ligands were synthesized to probe the steric and electronic demands required for use in the CuAAC reaction. Substituents on the 1,2,4-triazine were systematically altered and the core 1,2,4-triazine modified to determine the most active ligand. Additional experiments explored the variability in the reaction conditions, such as solvent choice, use of reducing agents, and optimal stoichiometry. Under optimum conditions 5,6-diphenyl-3-(2-pyridyl)-1,2,4-triazine and copper (II) tetrafluoroborate in the presence of triethylamine was found to …
Single-Grain Osl Chronologies For Middle Palaeolithic Deposits At El Mnasra And El Harhoura 2, Morocco: Implications For Late Pleistocene Human-Environment Interactions Along The Atlantic Coast Of Northwest Africa, Zenobia Jacobs, Richard Roberts, Roland Nespoulet, M El Hajraoui, Andre Debenath
Single-Grain Osl Chronologies For Middle Palaeolithic Deposits At El Mnasra And El Harhoura 2, Morocco: Implications For Late Pleistocene Human-Environment Interactions Along The Atlantic Coast Of Northwest Africa, Zenobia Jacobs, Richard Roberts, Roland Nespoulet, M El Hajraoui, Andre Debenath
Richard G Roberts
Optically stimulated luminescence (OSL) measurements were made on individual, sand-sized grains of quartz from Middle Palaeolithic deposits at two cave sites (El Harhoura 2 and El Mnasra) on the Atlantic coast of Morocco. We were able to calculate OSL ages for 32 of the 33 samples collected from the Middle Palaeolithic deposits, including the earliest and latest Aterian levels at both sites. These ages reveal periods of occupation between about 110 and 95 ka (thousands of years ago), and at ~75 ka. A late Middle Palaeolithic occupation of El Harhoura 2 is also recorded at ~55 ka. Our single-grain OSL …
2-(10′,10′-Dimethyl-3′-Sulfanylidene-4′- Azatricyclo[5.2.1.01,5]Decan-2′-Yl)-10,10-Dimethyl-4- Azatricyclo[5.2.1.01,5]Decane-3-Thione, Ashley Walker, Craig M. Forsyth, Patrick Perlmutter
2-(10′,10′-Dimethyl-3′-Sulfanylidene-4′- Azatricyclo[5.2.1.01,5]Decan-2′-Yl)-10,10-Dimethyl-4- Azatricyclo[5.2.1.01,5]Decane-3-Thione, Ashley Walker, Craig M. Forsyth, Patrick Perlmutter
Australian Institute for Innovative Materials - Papers
The title compound, C28H40N2O2S2, was obtained as a minor product from an anti-aldol reaction between the corresponding N-propionylthiolactam and benzaldehyde. The asymmetric unit contains one half-molecule, which is completed by inversion symmetry. The molecule displays a nearly eclipsed conformation along the central C-C bond with a C-C-C-C- torsion angle of 20.4 (3)°.
Direct Observation Of Domain Wall Motion And Novel Dielectric Loss In 0.23pb(In1/2nb1/2)O3-0.42pb(Mg1/3 Nb2/3)O3-0.35pbtio3 Crystals, Dabin Lin, Zhenrong Li, Fei Li, Shujun Zhang
Direct Observation Of Domain Wall Motion And Novel Dielectric Loss In 0.23pb(In1/2nb1/2)O3-0.42pb(Mg1/3 Nb2/3)O3-0.35pbtio3 Crystals, Dabin Lin, Zhenrong Li, Fei Li, Shujun Zhang
Australian Institute for Innovative Materials - Papers
Domain wall motion was directly observed at temperatures near to the monoclinic-to-tetragonal phase transition temperature (TM-T) in [001]-oriented 0.23Pb(In1/2Nb1/2)O3-0. 42Pb(Mg1/3Nb2/3)O3-0.35PbTiO3 (0.23PIN-0.42PMN-0.35PT) single crystals using a polarizing light microscope, and evident 90°and 180°domain switches were observed near the Curie temperature (TC). Two dielectric loss anomalies were observed at temperatures near TM-T in the [001]-oriented PIN-PMN-PT single crystals, while an additional dielectric loss peak was found at temperatures a few degrees below TC, which was associated with domain wall motion. Based on the domain structure observations, a domain switching mechanism was proposed to explain the novel dielectric loss peak at several degrees …
Polypyrrole Doped With Redox-Active Poly(2-Methoxyaniline-5-Sulfonic Acid) For Lithium Secondary Batteries, Yang Yang, Caiyun Wang, Syed A. Ashraf, Gordon G. Wallace
Polypyrrole Doped With Redox-Active Poly(2-Methoxyaniline-5-Sulfonic Acid) For Lithium Secondary Batteries, Yang Yang, Caiyun Wang, Syed A. Ashraf, Gordon G. Wallace
Australian Institute for Innovative Materials - Papers
Polypyrrole is a promising electrode material for flexible/bendable energy storage devices due to its inherent fast redox switching, mechanical flexibility, easy processability and being environmentally benign. However, its low attainable capacity limits its practical applications. Here, we synthesise a polypyrrole/poly(2-methoxyaniline-5-sulfonic acid) (PPy/PMAS) composite by incorporating redox-active PMAS into a PPy matrix via an electropolymerization method. For comparison, polypyrrole containing the electrochemically inert dopant p-toluenesulfonate (PPy-pTS) was prepared under the same conditions. The resultant PPy/PMAS film shows greatly improved electrochemical properties by harnessing the contribution from PMAS, i.e. higher specific capacity, better rate capability and improved cycling stability when used as …
Electrically Conductive Coatings Of Nickel And Polypyrrole/Poly(2- Methoxyaniline-5-Sulfonic Acid) On Nylon Lycra® Textiles, B C. Kim, P C. Innis, Gordon G. Wallace, C T.J Low, F C. Walsh, W J. Cho, K H. Yu
Electrically Conductive Coatings Of Nickel And Polypyrrole/Poly(2- Methoxyaniline-5-Sulfonic Acid) On Nylon Lycra® Textiles, B C. Kim, P C. Innis, Gordon G. Wallace, C T.J Low, F C. Walsh, W J. Cho, K H. Yu
Australian Institute for Innovative Materials - Papers
Woven nylon Lycra® has been coated with finely-divided electroless nickel-phosphorus, polypyrrole and electroless nickel/polypyrrole to produce flexible and electrically conductive textiles. The coated textiles were tested for their electrochemical activity, electrical resistivity and resistivity in response to mechanical strain. Pre-dyeing the textile with poly(2-methoxyaniline-5-sulfonic acid) (PMAS) prior to electroless metallization by electroless nickel and via chemical polymerization of polypyrrole was found to be beneficial in enhancing the resultant coating as well as stabilizing surface resistance responses when exposed to a wide range of strain. The mass gain due to the nickel coating was found to increase linearly with deposition time. …
Improved Dehydrogenation Properties Of The Combined Mg(Bh4) 2·6nh3-Nnh3bh3 System, Xiaowei Chen, Feng Yuan, Qinfen Gu, Yingbin Tan, Hua-Kun Liu, S X. Dou, Xuebin Yu
Improved Dehydrogenation Properties Of The Combined Mg(Bh4) 2·6nh3-Nnh3bh3 System, Xiaowei Chen, Feng Yuan, Qinfen Gu, Yingbin Tan, Hua-Kun Liu, S X. Dou, Xuebin Yu
Australian Institute for Innovative Materials - Papers
A combined strategy via mixing Mg(BH4)2·6NH3 with ammonia borane (AB) is employed to improve the dehydrogenation properties of Mg(BH4)2·6NH3. The combined system shows a mutual dehydrogenation improvement in terms of dehydrogenation temperature and hydrogen purity compared to the individual components. A further improved hydrogen liberation from the Mg(BH4)2·6NH3–6AB is achieved with the assistance of ZnCl2, which plays a crucial role in stabilizing the NH3 groups and promoting the recombination of NHδ+⋯HBδ−. Specifically, the Mg(BH4)2·6NH3–6AB/ZnCl2 (with a mole ratio of 1:0.5) composite is shown to release over 7 wt.% high-pure hydrogen (>99 mol%) at 95 °C within 10 min, thereby …
Crystallization, Phase Evolution And Ferroelectric Properties Of Sol-Gel-Synthesized Ba(Ti0.8zr0.2)O3- X(Ba0.7ca0.3)Tio3 Thin Films, Zeng-Mei Wang, Kuan Zhao, Xin-Li Guo, Wei Sun, Hua-Long Jiang, Xue-Qin Han, Xu-Tang Tao, Zhen-Xiang Cheng, Hong-Yang Zhao, Hideo Kimura, Guo-Liang Yuan, Jiang Yin, Zhi-Guo Liu
Crystallization, Phase Evolution And Ferroelectric Properties Of Sol-Gel-Synthesized Ba(Ti0.8zr0.2)O3- X(Ba0.7ca0.3)Tio3 Thin Films, Zeng-Mei Wang, Kuan Zhao, Xin-Li Guo, Wei Sun, Hua-Long Jiang, Xue-Qin Han, Xu-Tang Tao, Zhen-Xiang Cheng, Hong-Yang Zhao, Hideo Kimura, Guo-Liang Yuan, Jiang Yin, Zhi-Guo Liu
Australian Institute for Innovative Materials - Papers
A lead-free piezoelectric material with ultra-high properties, Ba(Ti0.8Zr0.2)O3-x(Ba0.7Ca0.3)TiO3(BZT-xBCT) nanocrystals was synthesized via a sol-gel method, and the corresponding thin films were also deposited on Pt/Ti/SiO2/Si substrates by a spin-coating approach. The BZT-xBCT thin film exhibited a high remnant polarization of 22.15 mC cm2 with a large coercive field of 68.06 kV cm1. The resultant gel is calcined at various elevated temperatures and studied with FTIR/XRD/Raman/DSC-TGA/AFM/SEM techniques for gel composition, crystallization, phase transition, thermochemistry and the morphology of the film. Although the room temperature crystal structure of the BZT-xBCT nanocrystals appears to be a standard perovskite structure by conventional X-ray diffraction …
Phase Gap In Pseudoternary R1-Yry Mn2x 2-Xxx Compounds, Jianli Wang, S J. Kennedy, S J. Campbell, M Hofmann, S X. Dou
Phase Gap In Pseudoternary R1-Yry Mn2x 2-Xxx Compounds, Jianli Wang, S J. Kennedy, S J. Campbell, M Hofmann, S X. Dou
Australian Institute for Innovative Materials - Papers
Our neutron diffraction investigation of PrMn2Ge2−xSix reveals a clear separation into two magnetic phases, canted ferromagnetic (Fmc) and antiferromagnetic (AFmc), between x = 1.0 and 1.2 and a commensurate phase gap in the lattice, due to magnetostrictive distortion. This remarkable magnetoelastic phenomenon is driven by a nonuniform atomic distribution on the X site which in turn produces subtle variations in the local lattice and abrupt changes in the Mn-Mn magnetic exchange interaction. Our results show that coexistence of Fmc and AFmc phases depends on lattice parameter, chemical pressure from the rare-earth and metalloid sites, and …
Colour Tunable Electrochromic Devices Based On Pprodot-(Hx)2 And Pprodot-(Ethx)2 Polymers, Bo Weng, Syed Ashraf, Peter C. Innis, Gordon G. Wallace
Colour Tunable Electrochromic Devices Based On Pprodot-(Hx)2 And Pprodot-(Ethx)2 Polymers, Bo Weng, Syed Ashraf, Peter C. Innis, Gordon G. Wallace
Australian Institute for Innovative Materials - Papers
The most commonly used method to tune the colour transition states of an ECD is to modify the chemical structure of the electrochromic polymers to achieve the desired transparent to dark state switching colours. However, this approach can present significant synthetic challenges that typically result in a compromise in device performance parameters such as contrast range or stability as well as solvent processability. In this study we have investigated tuning the dark-state colour of an ECD (at +0.8 V) by solution mixing poly(3,3-dihexyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine) (PProDOT-(Hx)2), which has an excellent contrast performance but with an esthetically undesirable purple colour transition, with poly(3,3-bis(2-ethylhexyl)-3,4-dihydro-2H-thieno …
Structure-Activity Relationship Of 2,3-Benzodiazepin-4-Ones As Noncompetitive Ampa Receptor Antagonists, Mohammad Shaban Qneibi
Structure-Activity Relationship Of 2,3-Benzodiazepin-4-Ones As Noncompetitive Ampa Receptor Antagonists, Mohammad Shaban Qneibi
Legacy Theses & Dissertations (2009 - 2024)
2,3-Benzodiazepin-4-one (BDZ-11) derivatives are a special group of 2,3-benzodiazepine compounds. These compounds have been previously synthesized as AMPA receptor inhibitors, and they are also potential drugs for the treatment of various neurological diseases involving excessive AMPA receptor activity. AMPA receptors are a subtype of glutamate ion channel proteins and are responsible for the majority of excitatory neurotransmission in the mammalian central nervous system. Specifically, they are critically involved in neuronal development and brain activities, including learning and memory. Overstimulation of AMPA receptors is associated with some neurological diseases such as ALS, stroke and Alzheimer's disease. Despite the fact that hundreds …
Electrochemistry Of 2,6-Diaminopurine On Multiwall Carbon Nanotube Modified Glassy Carbon Electrode, Ebru Mavi̇oğlu Ayan, Şükri̇ye Karabi̇beroğlu, Zekerya Dursun
Electrochemistry Of 2,6-Diaminopurine On Multiwall Carbon Nanotube Modified Glassy Carbon Electrode, Ebru Mavi̇oğlu Ayan, Şükri̇ye Karabi̇beroğlu, Zekerya Dursun
Turkish Journal of Chemistry
The electrochemical oxidation of 2,6-diaminopurine (2,6-DAP) was studied in pH 7.4 phosphate buffer solution on multiwall carbon nanotube modified glassy carbon electrode (MWCNT/GCE) over a temperature range of 20 to 50 °C using cyclic voltammetry. 2,6-DAP oxidation on MWCNT/GCE showed a well-defined and irreversible oxidation peak at about 0.72 V vs. Ag/AgCl at pH 7.4. The oxidation potential of 2,6-DAP linearly varied with pH over the range of 3.0 to 10.0 with a slope of --0.0547 V/pH, implying that 2 protons were accompanied by 2 electrons transferred in the electrochemical reaction. The activation energy, Ea, of oxidation reaction was found …
Synthesis And Biological Activities Of Methylenebis-4h-1,2,4-Triazole Derivatives, Yildiz Uygun, Hacer Bayrak, Havva Özkan
Synthesis And Biological Activities Of Methylenebis-4h-1,2,4-Triazole Derivatives, Yildiz Uygun, Hacer Bayrak, Havva Özkan
Turkish Journal of Chemistry
5,5'-Methylenebis(4--phenyl-4H-1,2,4-triazole-3-thiol) (2) was synthesized starting from hydrazinecarbothioamide compound (1). Treatment of compound 2 with ethyl bromoacetate produced diethyl 5,5'-{methylenebis[(4-phenyl-4H-1,2,4-triazole-5,3-diyl)thio]}diacetate (3), which was converted to the corresponding diacetohydrazide derivative (4) by treatment with hydrazine hydrate. The reaction of compound 4 with several aldehydes produced the corresponding arylidene hydrazides, 5a--d. Syntheses of Mannich bases 6a--c were carried out by the treatment of compound 2 with several amines in the presence of formaldehyde. (4{[5-({5-[(4-Amino-2-chlorophenyl)thio]-4-phenyl-4H-1,2,4-triazol-3-ylmethyl)-4-phenyl-4H-1,2,4-triazol-3-yl]thio}-3-chlorophenyl)amine (8) was prepared by reduction of 2 nitro groups of 3,3' -methylenebis{5-[(2-chloro-4-nitrophenyl)thio]-4-phenyl-4H-1,2,4-triazole} (7) that were obtained from the condensation of 2} with 3,4-dichloronitrobenzene. The newly synthesized compounds were screened …
Syntheses, Characterization, And Antibacterial Study Of Titanium Complexes, Raj Kaushal, Nitesh Kumar, Pamita Awasthi, Kiran Nehra
Syntheses, Characterization, And Antibacterial Study Of Titanium Complexes, Raj Kaushal, Nitesh Kumar, Pamita Awasthi, Kiran Nehra
Turkish Journal of Chemistry
Titanium(II) complexes of composition TiCl_2(L)_2 [where L = 2,2'-bipyridine (bipy), 4,4'-dimethyl-2,2'-bipyridine (bpMe), 4,4'-dimethoxy-2,2'-bipyridine (bpoMe), 6,6'-dimethyl-2,2'-bipyridine (dpMe), adamantylamine (ada)] were prepared by reacting titanium tetrachloride and N-containing bulky ligands in predetermined molar ratios. The complexes synthesized were characterized by different spectroscopic techniques, viz. UV-visible, FTIR, ^1H NMR, and mass spectrometry. The stoichiometry of the complexes was established by their elemental analysis (chlorine and titanium estimation). The unit cell parameters calculated by using the powder XRD tool confirm the monoclinic unit system and P lattice type for all complexes. Antibacterial screening of the ligands as well as the complexes was carried out …
Synthesis, Characterization, And Luminescence Of Zinc(Ii) And Cadmium(Ii) Coordination Complexes: [Zn(Phen)_2(Ch_3coo)](Clo_4), [Zn(Bpy)_2(Clo_4)](Clo_4), And [Cd(Phen)_2(No_3)_2], İbrahi̇m Kani̇, Mehmet Kurtça
Synthesis, Characterization, And Luminescence Of Zinc(Ii) And Cadmium(Ii) Coordination Complexes: [Zn(Phen)_2(Ch_3coo)](Clo_4), [Zn(Bpy)_2(Clo_4)](Clo_4), And [Cd(Phen)_2(No_3)_2], İbrahi̇m Kani̇, Mehmet Kurtça
Turkish Journal of Chemistry
Three metal complexes, [Zn(phen)_2(CH_3COO)](ClO_4) (1), [Zn(bpy)_2(ClO_4)](ClO_4) (2), and [Cd(phen)_2 (NO_3)_2] (3) (phen = 1,10-phenanthroline, bpy = 2,2 {Abedini, 2005 #222} -bipyridine), were synthesized and their structures were determined by single-crystal X-ray diffraction analyses. In 1, Zn(II) is coordinated by 4 nitrogen atoms from 2 phen molecules and 2 oxygen atoms from 1 acetato to form an octahedral configuration. In 2, Zn(II) has pentacoordination geometry with chelating 2 bpy and 1 perchlorato ion. In 3, phen and NO_3^- serve as bidentate ligands coordinating to Cd(II) through their nitrogen and oxygen atoms to form 8 coordination. Three-dimensional frameworks of complexes 1--3 are …