|
1. |
Spectral Investigations of thf Photoreactions of Flavomononucleotide (FMM) Immoblized in Polymer Film |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 495-508
R. Drabent,
M. Romanowski,
D. Frackowiak,
Preview
|
PDF (340KB)
|
|
摘要:
The absorption, fluorescence and photo-acoustic spectra of flavomonnnucleotide (FMM) molecules embedded in polyvinyl alcohol film were measured for illuminated and for stored in darkness samples. The effect of illumination depends an pigment concentration, and it is connected with FMN excimers formation. The FMN excimer formation prevented the photodestruction of isoatloxazine ring.
ISSN:0038-7010
DOI:10.1080/00387018808082325
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
2. |
The Mass Spectra and Disproportionation Studies of a Nitrogen Compound of Mercury (I) with 1,10 Phenanthroline |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 509-518
BassemF. Shraydeh,
Preview
|
PDF (203KB)
|
|
摘要:
A nitrogen compound of mercury (1) was prepared by reaction of 1,10 phenanthroline with mercurous nitrate. The mass spectra of this resulting precipitate was made and its distinguished features have been discussed. The results of various investigations suggest that disproportionation of the Hg(I) state did not occur.
ISSN:0038-7010
DOI:10.1080/00387018808082326
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
3. |
Separation of Components in Crystalline and Amorphous Regions of Polyethylene by Solid State Carbon-13 Nmr Spectroscopy |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 519-531
A.L. Cholli,
W.M. Ritchey,
J.L. Koenig,
V.S. Veeman,
Preview
|
PDF (355KB)
|
|
摘要:
The cross-polarization (CP) technique1–2, combined with magic angle sample spinning (MAS)3,4and high power decoupling5, usually provides high resolution spectra of solids2,6–8. These high resolution13C NMR spectra are in many cases sufficiently detailed to characterize the system9–17In the case of polyethylene (PE), it was shown that distinct conformations in the crystalline regions lead to a narrow crystalline resonance and the non-crystalline regions appear as a broad shoulder on the upfield side. 14 Since it is often difficult to obtain detailed information from unresolved spectra, it is either desirable to resolve these peaks or isolate one resonance peak from another by alteration of the measurement.
ISSN:0038-7010
DOI:10.1080/00387018808082327
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
4. |
Application of Proton Magnetic Resonance Spectrometry in the Analysis of Diclofenac Sodium and Its Tablets |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 533-539
S.A. Abdel Fattah,
S.Z. El-khateeb,
S.A. Abdel Razeg,
M.S. Tawakkol,
Preview
|
PDF (184KB)
|
|
摘要:
A new simple and rapid quantitative proton magnetic resonance method has been developed for the determination of diclofenac sodium in pure and tabler forms. Among other peaks, the PMR spectrum of diclofenac has a well defined sharp singlet (at ≃ 3.62 ppm) which is chosen for quantitative measurements. The method involves co-paring the integral of this signal to that of a sharp singlet of anhydrous sodium acetate (at ≃ 1.85 ppm) which is used as internal standard.
ISSN:0038-7010
DOI:10.1080/00387018808082328
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
5. |
5,5- Dimethyl -1,2,3 -Cyclohexanetrione 1.2- Dioxime 3 - Thiosemicarbazone as a Reagent for the Spectrophotometric Determination of Nickel and Copper |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 541-550
Radi Salim,
A.H. Laila,
A. Qamhieh,
Preview
|
PDF (273KB)
|
|
摘要:
The complexes of nickel and copper with the reagent 5,5-dimethyl -1,2-3- cyclohexanetrione 1,2,-dioxime 3-thiosemicarbazone have been studied. Properties of these complexes such as composition stability constant and free energy change of formation have been determined. These complexes have been used to develop spectrophotometric methods for the analysis of nickel and copper in aqueous solutions. Sensitivities and ranges of application of these methods have been determined. The optimum conditions for maximum sensitivity such as wavelength,pH and etanding time have been determined.The effect of foreign ions on these methods has been also investigated .
ISSN:0038-7010
DOI:10.1080/00387018808082329
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
6. |
Suppression of Signals from the Probe in NMR T1, Measurements |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 551-558
D.G. Cory,
W.M. Ritchey,
Preview
|
PDF (202KB)
|
|
摘要:
A simple method is described for accurately measuring spin lattice relaxation times in the presence of large probe background resonances. The method relies on selectively exciting those spins which are In the center of the rf coil, by employing pulse schemes which were developed for surface coil studies. The accuracy of the technique is checked by measurements on camphor in the solid state.
ISSN:0038-7010
DOI:10.1080/00387018808082330
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
7. |
The Use of the Protou Magnetic Pesonance (PMR) Spectroscopy in the Quantitative Determination of Dapsone in the Bulk and Tablets |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 559-564
IsisZ. F. Shukrallah,
AlfiB. Sakla,
Preview
|
PDF (192KB)
|
|
摘要:
A quantitative procedure for the determination of dapsone [80-08-0], I, in authentic mixtures and tablets, II, has been developed using the PMR spectroscopy. The comparison of the proposed PMR method with the official assays of the B.P. 1980 was achieved, and the results were statistically evaluated. The PMR determination is fairly accurate, more precise and providing advantageous traits regarding the simplicity and the rapidity of the method as well as the specificity of the technique in identifying and testing the purity of the compound.
ISSN:0038-7010
DOI:10.1080/00387018808082331
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
8. |
Two- Dimensional NMR Studies of Triterpenoid Glycosides.1H and13C NMR Assignments of Hederasaponin C [3-O-α-L-Rhamnopyranosyl-(1→2)-α-L-Arabinopyranosyl-Hederagenin 28-O-α-L-Rhamnopyranosyl-(l→4)-β-D-Glucopyranosyl-(1→6)-β-D-Glucopyranosylester] |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 565-573
A. Babadjamian,
R. Elias,
R. Faure,
E. Vidal-ollivier,
G. Balansard,
Preview
|
PDF (309KB)
|
|
摘要:
During an investigation of the triterpenoid glycosides constituents of Hedera helix we isolated the previously reported Hederasaponin C. Through the concerted application of 2D-homonuclear and heteronuclear chemical shift correlations total assignment of13C and1H NMR spectra was achieved.13C NMR data for two other saponins, Hederasaponin B and saponin K10, are also reported. Hederasaponin K10 was isolated for the first time in Hedera Helix leaves.
ISSN:0038-7010
DOI:10.1080/00387018808082332
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
9. |
Strong Hydrogen Bonding. Assignments in the Vibrational Spectra of the Isomorphous Salts: KHSO4, and KHSeO4 |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 575-587
A.W. Al-kassab,
B.D. James,
J. Liesegang,
I. Petrov,
V. Petrushevski,
B. Soptrajanov,
Preview
|
PDF (350KB)
|
|
摘要:
Despite the fact that khSO4and KHSeO4are isomorphous, the infrared spectra of these compounds are remarkably different. The characteristic 'A, B, C' trio is present in the spectrum of KHSeo4whereas multiplet structure of the o-H stretching band is found in KHSO4. On lowering the temperature, the bands in the 3000–2000 cm−1region become more structured and new bands appear in the 2000–1500 cm−1interval. Deuteration causes marked changes in the infrared spectra, as expected for strongly hydrogen bonded systems, although the Raman spectra are largely unaffected. Assignments in terms of separate R-O(H) and RO3units are presented.
ISSN:0038-7010
DOI:10.1080/00387018808082333
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
10. |
Centrifugal Distortion Constants and Potential Energy Curves of the InBr Molecule |
|
Spectroscopy Letters,
Volume 21,
Issue 7,
1988,
Page 589-596
N. Badowski,
Preview
|
PDF (202KB)
|
|
摘要:
Using: semiclassical calculation the centrifugal distortion constants have been obtained for the X1σ+, A3II0and B3II1electronic states of InBr.
ISSN:0038-7010
DOI:10.1080/00387018808082334
出版商:Taylor & Francis Group
年代:1988
数据来源: Taylor
|
|