119Sn, 13C and 1H NMR studies of aryloxy- and arylthio(1-butyl)stannanes

1989 ◽  
Vol 54 (9) ◽  
pp. 2386-2398 ◽  
Author(s):  
Antonín Lyčka ◽  
Jaroslav Holeček ◽  
Karel Handlíř
Keyword(s):  
Nmr Spectroscopy ◽  
Organic Compounds ◽  
1H Nmr ◽  
Organotin Compounds ◽  
Nmr Studies ◽  
Spectral Parameters ◽  
H Nmr ◽  
Mutual Comparison ◽  
Aromatic Systems

Two series of compounds have been prepared and studied by means of 119Sn, 13C, and 1H NMR spectroscopy, viz. aryloxy- and N-heteroaryloxytris(1-butyl)stannanes and their thio analogues Bu3SnER, and diaryloxy- and di(N-heteroaryloxy)bis(1-butyl)stannanes and their thio analogues Bu2Sn(ER)2, where E means oxygen or sulfur, Bu is 1-butyl, R = phenyl, 1-naphthyl, or 8-quinolyl. On the basis of mutual comparison of NMR spectral parameters of both series of organotin compounds and their comparison with NMR spectral parameters of analogous, purely organic compounds CH3ER it is possible to discuss the consequences of the presence of tin atoms in the organotin substituents and of nitrogen heteroatoms in the aromatic systems, and the therefrom following structure of the organotin compounds studied.

Conformational study on ribonucleoside O-phosphonylmethyl derivatives by 1H NMR spectroscopy

1985 ◽  
Vol 50 (8) ◽  
pp. 1899-1905 ◽  
Author(s):  
Milena Masojídková ◽  
Jaroslav Zajíček ◽  
Miloš Buděšínský ◽  
Ivan Rosenberg ◽  
Antonín Holý
Keyword(s):  
Nmr Spectroscopy ◽  
1H Nmr ◽  
1H Nmr Spectroscopy ◽  
Conformational Study ◽  
H Nmr ◽  
Conformational Properties

Conformational properties of ribonucleoside 5'-O-phosphonylmethyl derivatives have been determined by 1H NMR spectroscopy and compared with those of natural nucleosides and 5'-nucleotides.

Different submicellar solubilization mechanisms revealed by 1H NMR and 2D diffusion ordered spectroscopy (DOSY)

2020 ◽  
Vol 22 (19) ◽  
pp. 11075-11085
Author(s):  
Mengjian Wu ◽  
Zhaoxia Wu ◽  
Shangwu Ding ◽  
Zhong Chen ◽  
Xiaohong Cui
Keyword(s):  
Nmr Spectroscopy ◽  
Sodium Dodecyl Sulfate ◽  
1H Nmr ◽  
Sodium Dodecyl ◽  
Butyl Methacrylate ◽  
H Nmr ◽  
Molecular Scale ◽  
Two Systems ◽  
Dodecyl Sulfate ◽  
Triton X

Different submicellar solubilization mechanisms of two systems, Triton X-100/tetradecane and sodium dodecyl sulfate (SDS)/butyl methacrylate, are revealed on the molecular scale by 1H NMR spectroscopy and 2D diffusion ordered spectroscopy (DOSY).

scholarly journals Assessment of 1H NMR Spectroscopy for Specific Metabolite Fingerprinting of Angelica sinensis

2008 ◽  
Vol 3 (5) ◽  
pp. 1934578X0800300
Author(s):  
Dongmin Su ◽  
Jinglan Han ◽  
Shishan Yu ◽  
Hailin Qin
Keyword(s):  
Nmr Spectroscopy ◽  
1H Nmr ◽  
1H Nmr Spectroscopy ◽  
Nmr Spectra ◽  
Authentic Sample ◽  
Angelica Sinensis ◽  
Metabolite Fingerprinting ◽  
H Nmr ◽  
Pure Compounds ◽  
Polar Extracts

The 1H NMR fingerprints of fractionated non-polar extracts (CSPD A) from the roots of Angelica sinensis of six different specimens were assigned by comparison with the 1H NMR spectra of the isolated pure compounds. The 1H NMR fingerprints showed exclusively characteristic resonance signals of the major constituents of the plant. The 1H NMR fingerprint established for an authentic sample of A. sinensis can be used for authenticating A. sinensis species.

scholarly journals Synthesis of cis, cis-1,3,5-trisubstituted cyclohexane based chelators with polyfunctional pendant arms

2005 ◽  
Vol 2005 (1) ◽  
pp. 43-45 ◽  
Author(s):  
Minati Baral ◽  
B.K. Kanungo ◽  
Peter Moore
Keyword(s):  
Schiff Base ◽  
Nmr Spectroscopy ◽  
Organic Compounds ◽  
Elemental Analysis ◽  
H Nmr ◽  
Benzenetricarboxylic Acid ◽  
New Compounds ◽  
Pendant Arms ◽  
C Nmr

Some novel organic compounds of the type: cis, cis-1,3,5-tris(X)cyclohexane, where X= –CONH(CH2)2NH2, –CONH(CH2)3NH2, –CONH(CH2)2NCH –C6H4OH, CONH(CH2)3NCHC6H4OH, which are expected to function as potential polydentate chelators have been synthesised from 1,3,5-benzenetricarboxylic acid through multi-steps reactions. 1,3,5-benzenetricarboxylic acid was reduced to cis, cis-1,3,5-tris(ethylcarboxylate)cyclohexane, which on reaction with excess of 1,2-diaminoethane and 1,2-diaminopropane afforded two new compounds. Condensation of the obtained derivatives with three equivalents of salicylaldehyde resulted the formation of two new Schiff base compounds. All the compounds were characterised by a combination of elemental analysis, mass, IR, UV-Vis, 1H NMR and 13C NMR spectroscopy.

Low-field 1H-NMR spectroscopy for compositional analysis of multicomponent polymer systems

The Analyst ◽  
2019 ◽  
Vol 144 (5) ◽  
pp. 1679-1686 ◽  
Author(s):  
Sneha B. Chakrapani ◽  
Michael J. Minkler ◽  
Bryan S. Beckingham
Keyword(s):  
Nmr Spectroscopy ◽  
1H Nmr ◽  
1H Nmr Spectroscopy ◽  
Compositional Analysis ◽  
Polymer Systems ◽  
H Nmr ◽  
Low Field ◽  
Multicomponent Polymer

A low-field, 60 MHz, 1H NMR spectrometer yields quantitatively comparable results to 400 MHz spectrometers for the compositional analysis of multicomponent polymer systems.

N-Confused porphyrins: complexation and 1H NMR studies

2017 ◽  
Vol 41 (16) ◽  
pp. 7932-7937 ◽  
Author(s):  
Ilya A. Khodov ◽  
Olga V. Maltceva ◽  
Vladimir V. Klochkov ◽  
Oscar I. Koifman ◽  
Nugzar Zh. Mamardashvili
Keyword(s):  
Organic Solvents ◽  
1H Nmr ◽  
Nmr Studies ◽  
H Nmr ◽  
Vis Spectroscopy

The complexation of 2-aza-21-carba-tetraphenylporphyrin and 2-aza-2-methyl-5,10,15,20-tetraphenyl-21-carbaporphyrin with nickel and zinc acetates in organic solvents has been investigated by UV-Vis spectroscopy and 1H NMR.

Light induced E–Z isomerization in a multi-responsive organogel: elucidation from 1H NMR spectroscopy

2015 ◽  
Vol 51 (53) ◽  
pp. 10680-10683 ◽  
Author(s):  
Sanjoy Mondal ◽  
Priyadarshi Chakraborty ◽  
Partha Bairi ◽  
Dhruba P. Chatterjee ◽  
Arun K. Nandi
Keyword(s):  
Mechanical Properties ◽  
Nmr Spectroscopy ◽  
1H Nmr ◽  
1H Nmr Spectroscopy ◽  
Nmr Spectra ◽  
H Nmr ◽  
Imine Bond

Light induced E–Z isomerization along imine bond in a multiresponsive organogel of anthracene attached 3,4,5-tris(dodecyloxy)benzohydrazide gelator altering morphology, fluorescence and mechanical properties is elucidated from 1H NMR spectra.

scholarly journals 1H NMR spectroscopic elucidation in solution of the kinetics and thermodynamics of spin crossover for an exceptionally robust Fe2+ complex

2016 ◽  
Vol 45 (35) ◽  
pp. 13798-13809 ◽  
Author(s):  
Holm Petzold ◽  
Paul Djomgoue ◽  
Gerald Hörner ◽  
J. Matthäus Speck ◽  
Tobias Rüffer ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
1H Nmr ◽  
Spin Crossover ◽  
Kinetics And Thermodynamics ◽  
H Nmr ◽  
Spin Crossover Complexes

A series of exceptionally robust Fe2+ spin crossover complexes has been synthesized and investigated by 1H NMR spectroscopy in solution.

Analysis of 1H and 13C{1H} NMR Spectral Parameters of Diphenylchloroarsine, Diphenylcyanoarsine, and 10-Chloro- 5,10-Dihydrophenarsazine: Identification of the Compounds through Reference to Simulated Spectra

1997 ◽  
Vol 51 (5) ◽  
pp. 733-737 ◽  
Author(s):  
Markku Mesilaakso ◽  
Eeva-Liisa Tolppa ◽  
Paula Nousiainen
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
1H Nmr ◽  
Nmr Spectra ◽  
Spectral Parameters ◽  
H Nmr ◽  
Iterative Analysis ◽  
Simulation Of Spectra ◽  
Nuclear Magnetic

The 1H and 13C{1H} nuclear magnetic resonance (NMR) spectra of diphenylchloroarsine, diphenylcyanoarsine, and 10-chloro-5,10-dihydrophenarsazine were recorded from samples prepared in CDCl3, CD2Cl2, and (CD3)2CO. Spectra were analyzed, and detailed 1H NMR spectral parameters were determined by iterative analysis. Simulation of spectra and their use as reference spectra for identification of the compounds under different conditions are discussed.

scholarly journals NMR Studies of Lignins. 8. Examination of Pyridine-d5 Solutions of Acetylated Lignins from Birch and Spruce by 1H NMR Spectroscopy.

1986 ◽  
Vol 40b ◽  
pp. 791-797 ◽  
Author(s):  
Knut Lundquist ◽  
Sverker von Unge ◽  
Martin Nilsson ◽  
Curt R. Enzell ◽  
Jan-Eric Berg ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
1H Nmr ◽  
1H Nmr Spectroscopy ◽  
Nmr Studies
Sign in / Sign up

Export Citation Format

Share Document