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Full-Text Articles in Physical Sciences and Mathematics

Inept Nmr Spectroscopy Of ^{14}Nd_N Groups: Product Operator Theory And Simulation, Deni̇z Türkpençe, İrfan Şaka, Azmi̇ Gençten Jan 2010

Inept Nmr Spectroscopy Of ^{14}Nd_N Groups: Product Operator Theory And Simulation, Deni̇z Türkpençe, İrfan Şaka, Azmi̇ Gençten

Turkish Journal of Physics

Product operator formalism is widely used for the analytical description of multi-dimensional and multiple-pulse NMR experiments for the weakly coupled spin systems having spin-1/2 and spin-1 nuclei. The INEPT NMR experiment is a polarization transfer experiment including J-coupling. In this study, the INEPT NMR experiment was analytically investigated by using product operator theory for weakly coupled IS_n(^{14}ND_n) (I=1, S=1; n=1, 2, 3) spin systems. The obtained theoretical results represent the FID values of ^{14}ND_n groups. In order to make Fourier transform of the obtained FID values, a Maple program is used and then simulated spectra of the INEPT experiment are …


Isolation And Identification Of A New Acetildenafil Analogue Used To Adulterate A Dietary Supplement: Dimethylacetildenafil, Ali̇ Hakan Göker, Maksut Coşkun, Mehmet Alp Jan 2010

Isolation And Identification Of A New Acetildenafil Analogue Used To Adulterate A Dietary Supplement: Dimethylacetildenafil, Ali̇ Hakan Göker, Maksut Coşkun, Mehmet Alp

Turkish Journal of Chemistry

A new sildenafil analogue was found to have been added illegally to a dietary supplement marketed for the enhancement of sexual function. The structure was determined as 5-(2-ethoxy-5- {[4-(3,5-dimethyl)piperazin-1-yl]-acetyl}phenyl)-1,6-dihydro-1-methyl-3- propyl-7H-pyrazolo [4,3-d]pyrimidin-7-one. Owing to the inclusion of a dimethyl group in acetildenafil, the detected compound was called dimethylacetildenafil. The sample was purified with column chromatography. The IR, LC/MS (ESI), and completely assigned NMR data of dimethylacetildenafil are reported for the first time. The structure was compared with that of acetildenafil and the results showed that the ethyl substitution at the 4-position of the piperazine ring had been replaced by a 3,5-dimethyl …


Effect Of Various Substituents On Intramolecular 1,1-Vinylboration, Synthesis Of 1-Silacyclobutene Derivatives, Ezzat Khan, Bernd Wrackmeyer Jan 2010

Effect Of Various Substituents On Intramolecular 1,1-Vinylboration, Synthesis Of 1-Silacyclobutene Derivatives, Ezzat Khan, Bernd Wrackmeyer

Turkish Journal of Chemistry

The reaction of 1-boryl-1-alkenyl chlorosilane derivatives with alkynyllithium reagents [Li-C\equiv C-R^3 (R^3~=~Ph, SiMe_3)] at low temperature (--78 °C) affords alkenyl(alkyn-1-yl)silanes. These compounds are precursors of 1-silacyclobutene derivatives, which are formed via intramolecular 1,1-vinylboration. This reaction works for various groups at silicon (R^1/R^2: R^1 = H, Me, Ph; R^2 = Me, Ph) and at the C=C and C\equiv C units (R/R^3: R = ^nBu, Ph; R^3 = ^nBu, Ph, SiMe_3). The conversion into 1-silacyclobutene derivatives is incomplete only in the case of R^3 = SiMe_3. The reactions were monitored by NMR spectroscopy in order to elucidate the reaction mechanism, and the …