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.

Interfacial synthesis and characterization of L-lysinederived optically active poly(hydrazide-imide)s

e-Polymers ◽  
2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Saeed Zahmatkesh ◽  
Alireza Banaei ◽  
Ashkbous Yazdanpanah
Keyword(s):  
Specific Rotation ◽  
Viscosity Measurement ◽  
Optically Active ◽  
Synthesis And Characterization ◽  
Aprotic Solvents ◽  
Glass Transition Temperatures ◽  
H Nmr ◽  
Interfacial Synthesis ◽  
Ft Ir

AbstractSix novel poly(hydrazide-imide)s (PHIa-f) were prepared from the reaction of a novel L-lysine-derived chiral diacid, ethyl L-lysine-N,N'-ditrimellitoyl diacide (1), with six synthetic dihydrazides by interfacial polycondensation. These polymers have inherent viscosities in the range of 0.23 to 0.42 dl g-1, display optical activity, and are readily soluble in polar aprotic solvents. They start to decompose (T10%) above 248 ºC and display glass-transition temperatures at 164.37-210.20 0C All of the above polymers were fully characterized by UV, FT-IR and 1H NMR spectroscopy, elemental analysis, TGA, DSC, inherent viscosity measurement and specific rotation.

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.

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.

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.

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.

scholarly journals Synthesis and characterization of palladium(II) complexes with glycine coumarin derivatives

2016 ◽  
Vol 81 (12) ◽  
pp. 1383-1392
Author(s):  
Danijela Stojkovic ◽  
Alessia Bacchi ◽  
Davide Capucci ◽  
Milica Milenkovic ◽  
Bozidar Cobeljic ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Elemental Analysis ◽  
Water Solution ◽  
13C Nmr Spectroscopy ◽  
Synthesis And Characterization ◽  
Coumarin Derivatives ◽  
1H And 13C Nmr ◽  
X Ray ◽  
Ir And Nmr Spectroscopy

A Pd(II) complex with methyl 2-((1-(2,4-dioxochroman-3-ylidene)ethyl)amino)acetate was synthesized. The structures of both the ligand and Pd(II) complex were determined by elemental analysis, IR and NMR spectroscopy. Recrystallization of Pd(II) complex from DMF/water solution resulted in its hydrolysis and formation of dimethylamine-(2-((1-(2,4-dioxochroman-3-ylidene)ethyl)amino)acetato)palladium(II) complex, the structure of which was determined by elemental analysis, IR, 1H and 13C NMR spectroscopy, as well as X-ray analysis.

scholarly journals Synthesis and characterization of tris[butyl-(1-methyl-3phenyl-propyl)-dithiocarbamato]cobalt(III) seskvitoluen

2002 ◽  
Vol 67 (2) ◽  
pp. 123-126 ◽  
Author(s):  
Goran Kaludjerovic ◽  
Vesna Djinovic ◽  
Srecko Trifunovic ◽  
Ismet Hodzic ◽  
Tibor Sabo
Keyword(s):  
Nmr Spectroscopy ◽  
Electronic Absorption ◽  
Elemental Analysis ◽  
13C Nmr ◽  
Sodium Salt ◽  
13C Nmr Spectroscopy ◽  
Bidentate Ligand ◽  
Synthesis And Characterization ◽  
1H And 13C Nmr

Anew bidentate ligand butyl-(1-methyl-3-phenyl-propyl)-dithiocarbamate (bm?pdtc) was prepared, as the sodium salt. In the reaction of hexaaminecobalt(III) chloride with Nabm?pdtc, the corresponding tris[butyl-(1-methyl-3-phenyl-propyl)-dithiocarbamato]cobalt(III) [Co(bm?pdtc)3]?complex was prepared. The complex was characterized by elemental analysis, infrared, electronic absorption, 1H and 13C-NMR spectroscopy.

Synthesis and characterization of alkyl- and acyl-substituted oxime–phosphazenes

2005 ◽  
Vol 83 (12) ◽  
pp. 2039-2045 ◽  
Author(s):  
Erol Çil ◽  
Mustafa Arslan ◽  
Ahmet Orhan Görgülü
Keyword(s):  
Nmr Spectroscopy ◽  
Key Words ◽  
Elemental Analysis ◽  
Allyl Bromide ◽  
Ethyl Bromide ◽  
Synthesis And Characterization ◽  
Oxime Derivatives ◽  
High Yields

Two oxime–cyclophosphazenes were prepared from the hexakis(4-formylphenoxy)cyclotriphosphazene (2) and hexakis(4-acetylphenoxy)cyclotriphosphazene (8). The reactions of these oximes with ethyl bromide, allyl bromide, propanoyl chloride, and acriloyl chloride were studied. Hexasubstituted compounds were obtained from the reactions of hexakis{4-[(hydroxyimino)methyl]phenoxy}cyclotriphosphazene (3) with ethyl bromide (4), allyl bromide (5), and propanoyl chloride (6), however, the oxime groups on 3 rearranged to nitrile (7) in the reaction of 3 with acriloyl chloride. Hexasubstituted compounds were also obtained from the reactions of hexakis{4-[(1)-N-hydroxyethaneimidoyl]phenoxy}cyclotriphosphazene (9) with allyl bromide (11) and propanoyl chloride (12). Tetra- and penta-substituted products were obtained from the reactions of 9 with ethyl bromide (10) and acriloyl chloride (13), respectively. All products were generally obtained in high yields. The structures of the compounds were defined by elemental analysis, IR, 1H, 13C, and 31P NMR spectroscopy. Key words: hexachlorocyclotriphosphazene, phosphazene, oxime, oxime derivatives, oxime–phosphazenes.

scholarly journals Synthesis and Characterization of Cyclotriphosphazenes Bearing Six Bile Acid Arms

2009 ◽  
Vol 64 (5) ◽  
pp. 551-554 ◽  
Author(s):  
Giancarlo Fantin ◽  
Marco Fogagnolo ◽  
Pier Paolo Giovannini
Keyword(s):  
Bile Acid ◽  
Nmr Spectroscopy ◽  
Elemental Analysis ◽  
Synthesis And Characterization ◽  
Bile Acid Derivatives

Four novel cyclotriphosphazene bile acid derivatives (1 - 4) were prepared starting from hexakis[4- (chloromethyl)phenoxy]cyclotriphosphazene (8) as the scaffold. The structures of the compounds were defined by elemental analysis, IR and 1H, 13C and 31P NMR spectroscopy.

Synthese und Charakterisierung von Halogen-phosphor(III)- Derivaten des 8-Hydroxychinolins. Röntgenstrukturanalyse von 8-[Phenyl(chloro)-phosphito]-chinolin/ Synthesis and Characterization of Halogen-phosphorus(III) Derivatives of 8-Hydroxyquinoline. X -Ray Structure Analysis of 8-[Phenyl(chloro)phosphito]-quinoline

1993 ◽  
Vol 48 (1) ◽  
pp. 85-89 ◽  
Author(s):  
Lin Yang ◽  
Peter G. Jones ◽  
Reinhard Schmutzler
Keyword(s):  
Nmr Spectroscopy ◽  
Single Crystal ◽  
Diffraction Study ◽  
Elemental Analysis ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
New Compounds ◽  
Derivatives Of

The reaction of 8 -trimethylsiloxyquinoline, 2 with PCl3, PhPCl2, and PhPF2 has furnished the corresponding 8 -quinolyl halophosphite derivatives, 3-5 . The synthesis of two metal complexes, 8 and 9, of 4 with Au(I) and Pt(II) is described. The new compounds were characterized by elemental analysis and by 1H and 31P NMR spectroscopy. A single crystal X-ray diffraction study of 4 has been conducted; a short intramolecular P ··· N contact (230.9 pm) and a long P-Cl bond (218.7 pm) were observed.

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