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101.
Under the solvo-thermal conditions, two novel CdII mixed-ligand coordination materials with 2,6-(1,2,4-triazole-4-yl)pyridine(L1) and aromatic poly-carboxylic acid co-ligands such as 5-R-isophthalic acid (R = nitro, sulfo), namely [Cd(L1)(NO2-BDC)(H2O)2] · 2H2O ( 1 ) and [Cd(L1)(HSIP)(H2O)] · 4H2O ( 2 ) (NO2-H2BDC = 5-nitroisophthalic acid, H3SIP = 5-sulfobenzene -isophthalic acid) were successfully prepared. These CdII mixed-ligand coordination polymers 1 – 2 have been measured by crystal X-ray analysis, FT-IR spectra and powder X-ray diffraction analyses. In 1 , these seven-coordinate CdII atoms (Cd1) are inter-linked by didentate 5-nitroisophthalic acid ligands forming 1D chain structures. In 2 , these L1 and partially de-pronated HSIP2– are inter-linked by central CdII centers and are arranged into the unique 2D micro-porous metal-organic framework of 2 . Side view of 2 , it is noted that numerous oxygen atoms of un-coordinated carboxylate groups and coordinated SO3 groups protrude out and decorate the 2D framework of 2 . PXRD patterns of 1 and 2 sample is tested, which is consistent with the simulated PXRD diffraction pattern. Photoluminescence studies show that 2 is highly selective and sensitive to trace elements of Eu3+ with excellent Ksv value (7.86 × 104 m –1) and low detection limit (5.56 × 10–2 mM), which also provides a convenient method and platform for real-time detection of Eu3+. 相似文献
102.
Mahsa Armaghan Ezzat Najafi Tim-Oliver Knedel Walter Frank Christoph Janiak 《无机化学与普通化学杂志》2020,646(22):1861-1868
Three d10-transition-metal coordination compounds [Cd(tfpb)2(4-bpmh)]n ( 1 ), [Cd(9-aca)(NO3)(OHCH3)(4-bpmh)]n ( 2 ) and [Zn2(dpp)4(4-bpmh)] ( 3 ) with the bridging ligand 4-bpmh were synthesized [4-bpmh = 1,2-bis(pyridin-4-ylmethylene)hydrazine, tfpb = 4,4,4-trifluoro-1-phenylbutane-1,3-dionate, 9-aca = anthracene-9-carboxylate, dpp = 1,3-diphenylpropane-1,3-dionate]. Compounds 1 – 3 were characterized by FT-IR spectroscopy, elemental analysis, and structurally authenticated by X-ray crystallography. Compounds 1 – 3 are constructed by an O,O'-donor ligand including chelating β-diketonates (tfpb, dpp) in 1 and 3 and a carboxylate ligand (9-aca) in 2 in combination with a linear neutral bidentate and bridging N-ligand (4-bpmh). The assembly and action of the bridging 4-bpmh ligand leads to one-dimensional coordination polymers in 1 , 2 and to a dinuclear coordination complex in 3 . The structures and the solid-state supramolecular interactions for studying the crystal packing fashions of 1 – 3 were analyzed. The supramolecular interactions including hydrogen bonding, C–H ··· π, π ··· π, and C–F ··· π in 1 , 2 , and 3 were founded. 相似文献
103.
Shabbir Hussain Saqib Ali Saira Shahzadi Saroj K. Sharma Kushal Qanungo Muhammad Altaf 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):542-551
Abstract Organotin complexes with the general formulae R2SnL2, R2Sn(Cl)L, and R3SnL have been synthesized where R = CH3, n-C4H6, C6H5, C6H11, and L = 4-(hydroxy methyl)piperidine-1-carbodithioic acid. The newly synthesized complexes have been characterized by elemental analysis, IR, NMR (1H, 13C and 119Sn), and, for one example, a single crystal x-ray structure. The FT-IR data shows the bidentate nature of the ligand. This coordination behavior is also confirmed by semi-empirical study. In the solid state, diorganotin complexes exhibit the penta/hexacoordinated geometry, whereas the triorganotin(IV) complexes show the five coordinated geometry. 119Sn NMR data reveal that triorganotin(IV) complexes exhibit the four coordinated geometry in solution, whereas the diorganotin(IV) compounds show the higher coordination, probably five or six. X-ray diffraction analysis of complex (2) shows a square pyramidal geometry around the tin atom on the basis of τ value. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. GRAPHICAL ABSTRACT 相似文献
104.
De-Qing Shi Abudhaim Feras Yi Liu 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):2663-2673
In order to find high-acitivity and low-toxicity pesticidal lead compounds, a type of novel, asymmetric cyclic phosphorothonamides containing substituted pyridine were synthesized via the condensation reactions of 2-chloro-4-substitutedphenyl-5,5-dimethyl-1,3,2-dioxaphosphinane 2-sulfide with 3-aminomethylpyridine. The cis and trans isomers of the products were isolated by column chromatography on silica gel. The structures of the products were characterized by 1 H NMR, 31 P NMR, MS, and elemental analyses. The configuration of 3a was determined by X-ray diffraction analysis. The results of the preliminary bioassay showed that the new compounds possess potential fungicidal activities. 相似文献
105.
A. A. Aly 《Phosphorus, sulfur, and silicon and the related elements》2013,188(10):2395-2409
6-aminopyrazolo[3,4-b]pyridine-5-carbonitrile (2) was used as a precursor for the synthesis of a variety of pyrazolo[3,4-b][1,8]naphthyridines (3, 4) and pentaazacyclopenta[b]naphthalenes (5–10, 13, 14) via the initial addition to either the cyano or amino group followed by cyclization. Also, a series of heptaazadicyclopenta[a,g]naphthalenes (15–17) and heptaazacyclopenta[b]phenanthrenes (18, 19) were obtained via the interaction of 4-(dibenzothiophen-2-yl)-1,5-dihydro-5-imino-3-methyl-1-phenyl-1,2,6,8,9-pentaazacyclopenta[b]naphthalen-6-ylamine (14) with different reagents. The structures of the synthesized compounds were established by elemental and spectral analyses. 相似文献
106.
S. K. Srivastava Shailja Tomar Rupali Rastogi Richa Saxena 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):634-640
Six new substituted diphenyltin(IV) O,O′-alkylene dithiophosphates, (C6H5)2Sn(X)S(S) POGO [G = —CH2C(CH3)2CH2—, X = Cl (1), SCN (3), ClO4 (5); G = —CH2C (C4H9)(C2H5)CH2—, X = Cl (2), SCN (4), ClO4 (6)], were synthesized by the reaction of the corresponding ammonium salts of the O,O’-alkylene dithiophosphates with an appropriate organotin(IV) chloride. The compounds were characterized on the basis of elemental and spectral analyses (ESI mass spectrometry, IR, 1H, 13C, 31P, and 119Sn NMR). The presence of a four-coordinated Sn atom and monodentate O,O’-alkylene dithiophosphate moiety in compounds 1–4 as well as bidentate O,O’-alkylene dithiophosphate unit in compounds 5,6 is established. 相似文献
107.
Bogdan Boduszek Tomasz Olszewski Waldemar Goldeman Magdalena Konieczna 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4):787-795
The synthesis of a series of new pyridine aminomethylphosphinic acids is described. These compounds were obtained in the reaction of the corresponding pyridine aldehydes with primary amines and with ethyl phenylphosphinate, or methylphosphinate, in the presence of bromotrimethylsilane. In aqueous, strong acid solutions, pyridine aminophosphinic acids were split, forming the phenyl-, or methylphosphonic, acid and the corresponding secondary pyridyl-alkylamines. The kinetics of some observed cleavages were measured, and a mechanism of the cleavage has been proposed. 相似文献
108.
A short, practical, and efficient preparation of 2-(indol-3-yl)pyridine derivatives via a one-pot procedure of 3-cyanoacetylindole, chalcones, and ammonium acetate under microwave irradiation was described. All these compounds were obtained in good yield, and their structures were confirmed by 1H NMR, infrared, and elementary analysis. 相似文献
109.
A system consisting of tosyl chloride-dimethyl formamide-pyridine was found to ensure oxidation of poly(vinyl alcohol) and some molecular alcohols. 相似文献
110.
Metal-free synthesis of substituted imidazole [1,2-a]pyridines from deprotective N-(prop-2-yn-1-yl)pyridin-2-amines in water is elucidated. Electron releasing substituents on pyridine ring provided pure products in quantitative yields without separation by column chromatography. 相似文献