scholarly journals Synthesis and characterization of new Oxazine , Thiazine and Pyrazol derived from chalcones

2014 ◽  
Vol 11 (2) ◽  
pp. 477-485 ◽  
Author(s):  
Baghdad Science Journal
Keyword(s):  
Nmr Spectroscopy ◽  
Hydrazine Hydrate ◽  
Elemental Analysis ◽  
Potassium Hydroxide ◽  
1H Nmr Spectroscopy ◽  
Room Temperature ◽  
Potassium Hydroxide Solution ◽  
Synthesis And Characterization ◽  
Heterocyclic Derivatives

In this study, chalcones were synthesis by condensing 2-acetylpyridine with aromatic aldehyde derivatives in dilute ethanolic potassium hydroxide solution at room temperature according to Claisen-Schmidt condensation. After that, new heterocyclic derivatives such as Oxazine, Thiazine and Pyrazol were synthesis by reaction between chalcones with urea, thiourea and hydrazine hydrate respectively scheme 1. All these compounds wrer characterization by FTIR, 1H-NMR spectroscopy and elemental analysis.

Synthesis, Rheological Behavior and Mechanical Characterization of Structural Fast-Setting Geopolymers

2005 ◽  
Vol 498-499 ◽  
pp. 488-493
Author(s):  
Antonio Eduardo Martinelli ◽  
D.M.A. Melo ◽  
E.P. Marinho ◽  
T.W.J. Batista ◽  
R.G.S. Araújo ◽  
...  
Keyword(s):  
Potassium Hydroxide ◽  
Room Temperature ◽  
Mechanical Characterization ◽  
Potassium Hydroxide Solution ◽  
Inorganic Materials ◽  
Molar Ratio ◽  
Synthesis And Characterization ◽  
Polymeric Precursor ◽  
Rheological Characterization

Geopolymers are inorganic materials with ceramic characteristics that can be synthesized at room temperature from the setting of slurries. Their structure consists of aluminosilicate units that polymerize in alkaline environment. The setting rate and mechanical behavior of geopolymers strongly depends on the SiO2:Al2O3 molar ratio, polymeric precursor and polymerization cation. The present work reports the synthesis and characterization of 3.5:1 (SiO2:Al2O3) structural geopolymers prepared using either metakaolin (GPMK) or kaolin (GPK) as geopolymeric precursor in potassium hydroxide solution. GPMK depicted quick setting whereas GPK set only after 4 hours. The rheological characterization of the slurries revealed that plastic viscosity and yield point of GPK were 0.40 Pa.s and 14.2 Pa, respectively, whereas GPMK set instantly. The compressive strength of both geopolymers were measured after 24 hours and resulted in similar results, i.e., 4.6 MPa for GPMK and 4.4 MPa for GPK. The strength of both geopolymers was compatible to values typical of structural materials.

Synthesis and Characterization of Indolylfulgide Photochromic Colorants

2013 ◽  
Vol 821-822 ◽  
pp. 522-526
Author(s):  
Ning Ning Lv ◽  
An Guo Sang ◽  
Yan Zhang
Keyword(s):  
Nmr Spectroscopy ◽  
1H Nmr Spectroscopy ◽  
Room Temperature ◽  
Uv Light ◽  
Synthesis And Characterization ◽  
Indole Derivatives ◽  
Thermal Stabilities ◽  
Nmr Data ◽  
New Compounds

This paper describes the synthesis of two photochromic 2-indolyl-fulgides by stobbe condensation of the corresponding 2-acyl-1,3-dimethyl-indole derivatives with diethyl isopropylidene succinate in the presence of hexamethyldisilazane potassium. The overall yields was up to 41% for 3 steps. Both prepared compounds are sensitive to UV light and change colors upon irradiation. And the two fulgides can be switched back and forth 100 times without obvious degradation. Thermal stabilities of the fulgides in acetonitrile at room temperature for 30 days and at 80 °C for 12 h were measured using UV-vis and 1H NMR spectroscopy. The absorption spectra of both forms did not exhibit any sign of degradation. The NMR data indicated that no new compounds were detected. The utilization of these materials for use in photochromic textiles were discussed.

Synthesis and Characterization of Silver(I) and Gold(I) Complexes Bearing a Pyrido-annelated N-Heterocyclic Carbene: A Rare Example of a Cocrystal Containing Two Different Gold(I) Complexes

2014 ◽  
Vol 69 (11-12) ◽  
pp. 1188-1198 ◽  
Author(s):  
Margit Kriechbaum ◽  
Daniela Otte ◽  
Manuela List ◽  
Uwe Monkowius
Keyword(s):  
Mass Spectrometry ◽  
Nmr Spectroscopy ◽  
Aromatic Compound ◽  
Elemental Analysis ◽  
Room Temperature ◽  
Electronic Spectroscopy ◽  
Crystalline Material ◽  
Synthesis And Characterization ◽  
Aurophilic Interactions

Abstract The cyclohexyl-substituted imidazo[1,5-a]pyridin-2-ium hexafluorophosphate, 2a, has been prepared as precursor for the respective pyrido-annelated N-heterocyclic carbene. [(NHC)2Ag]PF6, 3, has been synthesized by the reaction of 2a with AgCl=KOH in dichloromethane (DCM). Unexpectedly, the reaction of 3 with (tht)AuBr yielded both (NHC)AuBr and [(NHC)Au(tht)]PF6 which formed a 1 : 1 cocrystal (4a,b). The complexes are aggregated to infinite chains, which are governed by both π-π stacking and weak aurophilic interactions. Subsequent oxidation of the co-crystalline material with CsBr3 gave (NHC)AuBr3, 5. All compounds were characterized by NMR spectroscopy, mass spectrometry and elemental analysis. Additionally, compounds 2a and 5 were investigated by electronic spectroscopy: 2a behaves like a typical aromatic compound exhibiting absorption and fluorescence bands attributable to π-π* transitions. The Au(III) complex 5 exhibits ligand-centered fluorescence at room temperature and both ligand-centered fluorescence and a weak phosphorescence at 77 K.

Synthesis and Characterization of Three Novel Nitrogen-containing Macrolides

2011 ◽  
Vol 66 (9) ◽  
pp. 930-934
Author(s):  
Xin Leng ◽  
Bingqin Yang ◽  
Yuanyuan Liu ◽  
Yi Xie ◽  
Jie Tong
Keyword(s):  
Nmr Spectroscopy ◽  
Hydrogen Bonds ◽  
1H Nmr Spectroscopy ◽  
Mass Spectra ◽  
Synthesis And Characterization ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
Preparation Methods ◽  
X Ray

Three novel nitrogen-containing macrolides have been synthesized by esterification. All of them have been characterized by infrared (IR), elemental analysis, mass spectra (MS), and 1H NMR spectroscopy, and their crystal structures were determined by single-crystal X-ray diffraction. The preparation methods and the intermolecular associations based on C-H・・・O hydrogen bonds and π- π stacking interactions are discussed.

The Synthesis and Characterization of Nitrooxy- and Nitrosooxyborazine Compounds

2014 ◽  
Vol 69 (11-12) ◽  
pp. 1241-1247
Author(s):  
Thomas M. Klapötke ◽  
Magdalena Rusan
Keyword(s):  
Mass Spectrometry ◽  
Nmr Spectroscopy ◽  
Vibrational Spectroscopy ◽  
Elemental Analysis ◽  
Experimental Results ◽  
Synthesis And Characterization ◽  
The Impact

Abstract B-Nitrosooxypentamethylborazine, B-nitrooxypentamethylborazine and B-trinitrooxy-N-trimethylborazine have been synthesized and characterized by 1H, 13C, 11B, and 14N NMR spectroscopy, mass spectrometry, vibrational spectroscopy and elemental analysis. The 11B NMR shifts were calculated and compared to the experimental results. The decomposition temperatures and the impact and friction sensitivities of these compounds have been determined as well.

scholarly journals Synthesis and Characterization of New Silver (I) N-Heterocyclic Ccarbene Ccomplex Dderived from Imidazol-2-ylidene salt

2018 ◽  
Vol 28 (2) ◽  
pp. 55
Author(s):  
Mohammedl Mujbe Hasson
Keyword(s):  
Mass Spectrometry ◽  
Nmr Spectroscopy ◽  
13C Nmr ◽  
Room Temperature ◽  
13C Nmr Spectroscopy ◽  
Synthesis And Characterization ◽  
Imidazolium Salt ◽  
In Situ Method

A new N, N'-imidazolium salt 1-(2,6-diisopropylphenyl)-3- (4,6-dimorpholino -1,3,5-traizine-2-yl)-1H-imidazol-3-ium chloride) as a precursor of N - heterocyclic carbene ligand was prepared via the reaction of 1 - (2, 6 - diisopropyl phenyl - 1H - imidazole) with 1, 3, 5 - triazine derivative bearing morpholine substituent (2, 6 -dimorpholine - 6- chloro-1, 3, 5-triaziazine). Linear coordi-nated Ag (І) NHC complex was synthesised via deprotonation of the imidazolium salt and reac-tion with Ag2O in darkness at room temperature by in situ method. The complex was synthesised for using as transfer agent to prepare another transition metals complexes by transmetallation method in the future. The imidazolium salt and their silver complex have been characterized by 1 H and 13C NMR spectroscopy as well as mass spectrometry.

Synthesis and Characterization of the nido-Platinaborane 7,7-(PPh3)2-7-PtB10H11-11-OC(O)Me

2011 ◽  
Vol 66 (4) ◽  
pp. 387-391
Author(s):  
Jinling Miao ◽  
Yong Nie ◽  
Haiyan Chen ◽  
Daqi Wang ◽  
Markus Enders ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Hydrogen Bonds ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Chain Structure ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ir And Nmr Spectroscopy

The reaction of closo-B10H102− with PtCl2(PPh3)2 in the presence of MeCOSH afforded the title platinaborane nido-7,7-(PPh3)2-7-PtB10H11-11-OC(O)Me (1), which has been characterized by IR and NMR spectroscopy, MS, elemental analysis, and single-crystal X-ray diffraction. In contrast to the known products having exo-polyhedral Pt-S-C-O-B ring(s) from the same reaction with Ph- COSH, compound 1 has a B-acetoxy group on the open PtB4 face of the nido-PtB10 cluster. The structure of 1 features both intramolecular/intermolecular C-H· · ·O hydrogen bonds and intramolecular C-H· · ·H-B dihydrogen bonds, which link the molecules into a 1-D chain structure.

scholarly journals Synthesis and Characterization of New Optically Active Poly (ethyl L-lysinamide)s and Poly (ethyl L-lysinimide)s

2010 ◽  
Vol 2010 ◽  
pp. 1-6 ◽  
Author(s):  
Saeed Zahmatkesh ◽  
Mohammad Reza Vakili
Keyword(s):  
Nmr Spectroscopy ◽  
Elemental Analysis ◽  
Specific Rotation ◽  
Viscosity Measurement ◽  
Optically Active ◽  
Inherent Viscosity ◽  
Synthesis And Characterization

Ethyl L-lysine dihydrochloride was reacted with three different dianhydrides to yield the poly (ethyl L-lysinimide)s ( NMR spectroscopy, elemental analysis, WAX diffraction, TGA, inherent viscosity measurement, and specific rotation.

scholarly journals Design, Synthesis and Characterization of Novel Arylamides Containing 1,2,4-triazole Nuclei for Possible Antimicrobial Activity

2004 ◽  
Vol 1 (5) ◽  
pp. 228-230 ◽  
Author(s):  
S. R. Dhol ◽  
P. M. Gami ◽  
R. C. Khunt ◽  
A. R. Parikh
Keyword(s):  
Antimicrobial Activity ◽  
Hydrazine Hydrate ◽  
Carbon Disulfide ◽  
Acid Chloride ◽  
Potassium Hydroxide ◽  
Synthesis And Characterization ◽  
Design Synthesis ◽  
Elemental Analyses

Diphenyl aceto hydrazide on reaction with carbon disulfide and potassium hydroxide gave potassiumα,α-diphenyl acetamido dithiocarbamate, which on cyclisation with hydrazine hydrate yielded key intermediate 3-mercapto-4,N-amino-5-benzhydryl-1,2,4-triazoles. The key intermediate on condensation with different acid chloride afforded our titled compounds. The synthesised compounds have been confirmed elemental analyses and further supported by spectral data. All the synthesised compounds have been evaluated for theirin vitroin vitro antimicrobial activity.

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