Synthesis and characterization of a new Keggin anion: [BeW12O40]6−

2014 ◽  
Vol 50 (65) ◽  
pp. 9083-9085 ◽  
Author(s):  
Alexander V. Anyushin ◽  
Anton I. Smolentsev ◽  
Dmitry A. Mainichev ◽  
Cristian Vicent ◽  
Artem L. Gushchin ◽  
...  

The first berillododecatungstate [BeW12O40]6− has been synthesized and characterized by X-ray analysis, cyclic voltammetry, ESI-mass spectrometry, and 9Be and 183W NMR.

Synthesis ◽  
2019 ◽  
Vol 51 (10) ◽  
pp. 2116-2121 ◽  
Author(s):  
Wen-Rong Xu ◽  
Xin-Rui Wang ◽  
Hak-Fun Chow ◽  
Dietmar Kuck

A pair of enantiomerically pure metallodimers containing two deeply concave tribenzotriquinacene (TBTQ) units linked by a platinum-diacetylene unit were synthesized. Such linear metal-centered TBTQ dimers are considered as edges of metallosquares and metallocubes that bear four or eight mutually syn-oriented TBTQ bowls at their tips, respectively. The structures of the metallodimers were characterized by 1H, 13C and 31P NMR spectroscopy, ESI mass spectrometry, and circular dichroism. The single X-ray crystal structure of (+)-enantiomer confirmed the absolute configuration of the metallodimers and revealed an edge (tip-to-tip) length of 18.456 Å and an approximated syn-orientation of the two TBTQ bowls in the solid state.


2004 ◽  
Vol 57 (3) ◽  
pp. 269 ◽  
Author(s):  
Aston A. Eagle ◽  
Charles G. Young ◽  
Edward R. T. Tiekink

The missing member of the series Tp*ME(S2CNEt2) (M = Mo, W; E = O, S), namely Tp*WO(S2CNEt2), has been synthesized by oxygen-atom transfer from pyridine N-oxide to Tp*W(S2CNEt2)(CO)2. The air-stable, blue-purple complex was characterized by microanalysis, mass spectrometry (m/z 645 (100%), [M]+), cyclic voltammetry, and IR and 1H NMR spectroscopy. Solutions of the complex are dichroic and solvatochromic. The X-ray crystal structure of the complex revealed a six-coordinate, distorted octahedral complex with axial oxo (W = O 1.680(5) Å), ‘equatorial’ dithiocarbamate (W—S 2.3962(17) and 2.4102(17) Å), and facial tridentate Tp* ligands. The synthesis and characterization of Tp*WCl3 are also reported.


2015 ◽  
Vol 1784 ◽  
Author(s):  
Venkata Neti

ABSTRACTA series of fluorine appended highly conjugated fullerenes were prepared containing fluoro-α-cyanostilbene and aryl ester units. These modified PCBM dyads are fully characterized by NMR, Mass spectrometry, UV-vis, and cyclic voltammetry (Figures 1-4). It was found that the presence of fluoro-α-cyanostilbenes and esters affects the cyclic voltammetry and absorption in the UV-Vis region. The PCBA modified fullerenes significantly influences the HOMO-LUMO energy and wide absorption compared to PCBM.


Synthesis ◽  
2017 ◽  
Vol 49 (11) ◽  
pp. 2389-2393 ◽  
Author(s):  
Stefanie Pelzer ◽  
Beate Neumann ◽  
Hans-Georg Stammler ◽  
Nikolai Ignat’ev ◽  
Reint Eujen ◽  
...  

This paper describes the synthesis and comprehensive characterization of tetrakis(pentafluoroethyl)germane. In addition to a complete NMR spectroscopic characterization, including the rarely used 73Ge NMR spectroscopy, Ge(C2F5)4 was studied by IR spectroscopy, mass spectrometry as well as X-ray diffraction analysis. A 73Ge NMR investigation as well as an X-ray diffraction study of the related germane Ge(CF3)4 are also included.


2011 ◽  
Vol 66 (9) ◽  
pp. 947-952
Author(s):  
Meiling Xu ◽  
Yong Nie ◽  
Jinling Miao ◽  
Zhenwei Zhang ◽  
Bin Peng ◽  
...  

The reactions of the dithiolato-o-carborane salt (Et3NH)2(S2C2B10H10) (2) with alkyl halides BrCH2CH=CH2, BrCH2CH2CH2Cl and C6H5CH2Cl, afford the o-carboranyl-bisthioether derivatives 3a - c, which have been characterized by IR and NMR (1H, 13C, 11B) spectroscopy, mass spectrometry, and single-crystal X-ray diffraction (3c). The photoluminescent properties of the known compound 3c has been investigated. It exhibits a violet (chloroform solution) or blue (solid state) emission when excited with UV light.


1996 ◽  
Vol 51 (10) ◽  
pp. 1494-1500 ◽  
Author(s):  
Vasily A . Pinchuk ◽  
Ion Neda ◽  
Christian Müller ◽  
Holger Thönnessen ◽  
Peter G. Jones ◽  
...  

The reaction of 1,5-bis(trimethylsilyl)-1,3.5-trimethylbiuret (1) with p-tolylsulfenyl chloride (2) furnished l-(p-tolylthio)-5-trimethylsilyl-1,3,5-trimethylbiuret (3). In the reaction of 3 with phenyldichlorophosphine, 2-phenyl-2-(p-tolylthio)-1,3,5-trimethyl-1,3,5-triaza-4,6-dione- 2-phosphorinonium chloride (4) was formed. The same product was obtained from the reaction of 2-phenyl-1,3,5-trimethyl-1,3,5-triaza-2λ3- phosphorin-4,6-dione (6) with p-tolylsulfenyl chloride (2). Compound 4 was isolated and characterized in the form of the hexachloroantimonate (4a). The spirophosphorane 2-phenyl-1,3,5-trimethyl-1,3,5-triaza-7,10-dioxa-8,9- perchlorobenzo-2λ5-phosphaspiro-[4.5]decan-4,6-dione (7) was prepared by the reaction of 4 with tetrachloroorthobenzoquinone. The new products were characterized by 1H - and 13C NMR spectroscopy, elemental analysis, 31P NMR spectroscopy in the case of 4a. 6 and 7, and mass spectrometry (4a). Single-crystal X-ray structural analyses of compounds 4a and 7 were conducted. The phosphorus atom of 4a has the expected tetrahedral geometry, with a rather short P-S bond of 204.9(2) pm. In 7 the geometry at phosphorus is almost ideal trigonal bipyramidal. Weak hydrogen bonds are formed from a C (:O) group to deuterochloroform of solvation.


2016 ◽  
Vol 64 (2) ◽  
pp. 127-133
Author(s):  
Humaira Yeasmin ◽  
MS Rahman ◽  
AA Shaikh ◽  
Pradip K Bakshi

The complexes of Cu(II), Zn(II), Cd(II) and Hg(II) with adenine (AdeH) and uracil (UraH) have been synthesized and characterized by a combination of metal contents estimation, IR, UV-vis spectral data, thermogravimetric analysis (QSTG, TG and DSC) and magnetic susceptibility measurement. All the complexes are micro-crystalline, slightly soluble in water and decompose at high temperature. Both adenine and uracil deprotonated under experimental condition and then ligated to the metal ions as bidentate ligands through N(3) and N(9) of adeninato (Ade), and through N(3) and C(2)=O of uracilato (Ura) anions. On the basis of the metal contents, the complexes are formulated as [M(C5H4N5O)(C5H4N5)(H2O)2] [M = Cu(II), Zn(II) and Hg(II)] and [Cd(C5H4N5)(C4H3N2O2)(H2O)2].2H2O. The redox properties of copper and cadmium complexes were examined in aqueous solution by cyclic voltammetry. The voltammograms show quasi-reversible behavior for both the complexes. The X-ray powder diffraction study of the copper complex indicates that it is poorly crystalline in nature. Dhaka Univ. J. Sci. 64(2): 127-133, 2016 (July)


2013 ◽  
Vol 29 ◽  
pp. 28-33
Author(s):  
B. Shakya ◽  
P. N. Yadav

Pyrrolidine-1-carbothiohydrazide was prepared by the transamination reaction of 4-methyl-4-phenyl-3-thiosemicarbazide with pyrrolidine in MeCN. 2-pyridineformamide 3-pyrrolidinyl-thiosemicarbazone (HAmPyrr) was synthesized by the reduction of cyanopyridine in the presence of pyrrolidine-1-carbothiohydrazide in MeOH with Na metal. The synthesized compound was characterized by elemental analysis, IR, 1H-NMR, 13C-NMR spectroscopy and ESI mass spectrometry. The prominent (M+1) peak (m/z) of HAmPyrr in the electron spray ionization mass spectrum was found at 250.09 which correspond to the molecular ion plus H. DOI: http://dx.doi.org/10.3126/jncs.v29i0.9234Journal of Nepal Chemical SocietyVol. 29, 2012Page: 28-33Uploaded date : 12/3/2013


2019 ◽  
Vol 43 (28) ◽  
pp. 11209-11221 ◽  
Author(s):  
Cássia de Q. O. Cavalcante ◽  
Daniel da S. Arcanjo ◽  
Guilherme G. da Silva ◽  
Diêgo M. de Oliveira ◽  
Claudia C. Gatto

We report the synthesis and characterization of metal complexes with dithiocarbazates and the cytotoxicity against the breast cancer line MDA-MB-231.


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