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71.
Alexandru C. Razus Liviu Birzan Mihaela Cristea Eugenia Andreea Dragu Anamaria Hanganu 《Monatshefte für Chemie / Chemical Monthly》2011,40(9):1271-1282
Abstract
Two synthesis strategies were used for the generation of azulene-1-yl diazenes substituted at C-3 with a phenyl-chalcogenyl moiety, the synthesis of azulenes substituted at C-3 followed by azo-coupling and azulene substitution at C-3 in azulene-azo dyes. The last synthetic route seems to give more satisfactory results for the synthesis of the desired chalcogenic derivatives. Another target of this study was to investigate the changes induced by the phenyl-chalcogenic substitution on the NMR and UV-vis spectra, and also to compare this effect with the one exerted by halogen atoms and by strongly electron donating groups such as AcNH or PhCOO. Whereas the latter groups exhibit a strong influence on the NMR and UV-vis spectra, PhS, PhSe, or PhTe groups as well as halogen atoms produce only a small effect because of the moderate change in electron distribution over the entire molecule. 相似文献72.
Simple and low cost biosensor based on screen-printed electrode for sensitive detection of some alkylphenols was developed, by entrapment of HRP in a nanocomposite gel based on single-walled carbon nanotubes (SWCNTs) and 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF6]) ionic liquid. Raman and FTIR spectroscopy, CV and EIS studies demonstrate the interaction between SWCNTs and ionic liquid. The nanocomposite gel, SWCNT-[BMIM][PF6] provides to the modified sensor a considerable enhanced electrocatalytic activity toward hydrogen peroxide reduction. The HRP based biosensor exhibits high sensitivity and good stability, allowing a detection of the alkylphenols at an applied potential of −0.2 V vs. Ag/AgCl, in linear range from 5.5 to 97.7 μM for 4-t-octylphenol and respectively, between 5.5 and 140 μM for 4-n-nonylphenol, with a response time of about 5 s. The detection limit was 1.1 μM for 4-t-octylphenol, and respectively 0.4 μM for 4-n-nonylphenol (S/N = 3). 相似文献
73.
Rodica Olar Mihaela Badea Dana Marinescu Larisa Calu Cristina Bucur 《Journal of Thermal Analysis and Calorimetry》2011,105(2):571-575
Novel complexes of type [M2LCl4]·nH2O ((1) M:Ni, n = 5; (2) M:Cu, n = 0 and (3) M:Zn, n = 2; L: ligand resulted from 1,2-phenylenediamine, 3,6-diazaoctane-1,8-diamine and formaldehyde template condensation) were
synthesised and characterised. The features of complexes have been assigned from microanalytical, IR and UV–Vis data. The
thermal analyses have evidenced the thermal intervals of stability and also the thermodynamic effects that accompany them.
Processes as water or hydrochloric acid elimination as well as oxidative degradation of the organic ligand were observed.
Complexes display a different thermal behaviour as result of dissimilar chemical interaction of metal ions with chloride anions.
The final product of decomposition was metal(II) oxide as powder X-ray diffraction indicated. 相似文献
74.
Mihaela Badea Rodica Olar Valentina Uivarosi Dana Marinescu Victoria Aldea Stefania Felicia Barbuceanu George Mihai Nitulescu 《Journal of Thermal Analysis and Calorimetry》2011,105(2):559-564
Two new complexes having general formula VOL2·nH2O [(1) L: 5-hydroxyflavone, n = 1; (2) L: chrysin, n = 4] were synthesized and characterized. Based on IR and electronic data we concluded that studied flavones act as bidentate
ligands in complexes with metallic ion coordinated in a square-pyramidal stereochemistry. The thermal analysis (TG, DTA) elucidated
the composition and also the number and nature of the water molecules. The thermal behavior also indicated strong interactions
between oxovanadium (IV) and these oxygen donor ligands. 相似文献
75.
Let V
n
be the SL2-module of binary forms of degree n and let V = Vn1 ???Vnp V = {V_{{n_1}}} \oplus \cdots \oplus {V_{{n_p}}} . We consider the algebra
R = O(V)\textS\textL2 R = \mathcal{O}{(V)^{{\text{S}}{{\text{L}}_2}}} of polynomial functions on V invariant under the action of SL2. The measure of the intricacy of these algebras is the length of their chains of syzygies, called homological dimension hd R. Popov gave in 1983 a classification of the cases in which hd R ≤ 10 for a single binary form (p = 1) or hd R ≤ 3 for a system of two or more binary forms (p > 1). We extend Popov’s result and determine for p = 1 the cases with hd R ≤ 100, and for p > 1 those with hd R ≤ 15. In these cases we give a set of homogeneous parameters and a set of generators for the algebra R. 相似文献
76.
M. F. Lazarescu D. Pantelica A. S. Manea R. V. Ghita F. Negoita 《Journal of Crystal Growth》2002,240(3-4):401-406
We found Oxygen-doped GaAs crystals to be suitable materials for CO2 laser optical component preparation, with application at 10.6 μm. An optical transmission of 55% in the IR spectrum range, between 2 and 15 μm has been reached for such a GaAs type material. The GaAs crystals that we have analysed were grown by two procedures: Horizontal Bridgman (HB) and Liquid Encapsulated Czochralski (LEC). The HB method has been used for obtaining pure (undoped) crystals, while the oxygen-doped GaAs ingots were grown by LEC technique. The two types of samples processed in the same manner as regards mechanical polishing and chemical etching, which were investigated by Hall measurements, optical transmission spectrometry and elastic recoil detection analysis (ERDA) technique. The GaAs:O (LEC) has near semi-insulating properties as can be observed from the results of the electrical resistivity and Hall effect measurements. The ERDA spectrum shows an intense signal of oxygen in the bulk of GaAs:O (LEC) crystals, while the oxygen signal is not present in the ERDA spectrum of the undoped GaAs (HB). We consider that these results could recommend the ERDA technique as a possible qualitative and quantitative analysis in an ion-beam accelerator for oxygen content in oxygen-doped GaAs crystals. The analysis is not sensitive to the native oxide, as could be seen by measuring GaAs (HB) undoped crystals. 相似文献
77.
78.
Multivalent Recognition of Concanavalin A by {Mo132} Glyconanocapsules—Toward Biomimetic Hybrid Multilayers 下载免费PDF全文
Dr. Mihail Barboiu Dr. Zineb Mouline Dr. Mihaela Silion Erol Licsandru Prof. Bogdan C. Simionescu Dr. Eugene Mahon Dr. Mariana Pinteala 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(22):6678-6683
Herein, we consider Müller’s spherical, porous, anionic, molybdenum oxide based capsule, (NH4)42‐ [{(MoVI)MoVI5O21(H2O)6}12{MoV2O4(CH3COO)}30]?10 CH3COONH4? 300 H2O≡(NH4)42? 1 a ?crystal ingredients≡ 1 , {Mo132}, as an effective sugar‐decorated nanoplatform for multivalent lectin recognition. The ion‐exchange of NH4+ ions of 1 with cationic‐sugars, D ‐mannose‐ammonium chloride ( 2 ) or D ‐glucose‐ammonium chloride ( 3 ) results in the formation of glyconanocapsules (NH4)42?n 2 n? 1 a and (NH4)42?m 3 m? 1 a . The Mannose (NH4)42?n 2 n? 1 a capsules bind selectively Concanavalin A (Con A) in aqueous solution, giving an association avidity constant of ${K{{{\rm multi}\hfill \atop {\rm a}\hfill}}}$ =4.6×104 M ?1 and an enhancement factor of β=K${{{{\rm multi}\hfill \atop {\rm a}\hfill}}}$ /K${{{{\rm mono}\hfill \atop {\rm ass}\hfill}}}$ =21.9, reminiscent of the formation of “glycoside clusters” on the external surface of glyconanocapsule. The glyconanocapsules (NH4)42?n 2 n? 1 a and (NH4)42?m 3 m? 1 a self‐assemble in “hybrid multilayers” by successive layer‐by‐layer deposition of (NH4)42?n 2 n? 1 a or (NH4)42?m 3 m? 1 a and Con A. These architectures, reminiscent of versatile mimics of artificial tissues, can be easily prepared and quantified by using quartz crystal microgravimetry (QCM). The “biomimetic hybrid multilayers” described here are stable under a continual water flow and they may serve as artificial networks for a greater depth of understanding of various biological mechanisms, which can directly benefit the fields of chemical separations, sensors or storage‐delivery devices. 相似文献
79.
Tao C Deselnicu M Fan H Mukarakate C Ionescu I Reid SA 《Physical chemistry chemical physics : PCCP》2006,8(6):707-713
To further investigate the Renner-Teller (RT) effect and barriers to linearity and dissociation in the simplest singlet carbene, we recorded fluorescence excitation spectra of bands involving the pure bending levels 2(n)(0) with n = 0-9 and the combination states 1(1)(0)2(n)(0) with n = 1-8 and 2(n)(0)3(1)(0) with n = 0-5 in the A(1)A'<-- X(1)A' system of CDF, in addition to some weak hot bands. The spectra were measured under jet-cooled conditions using a pulsed discharge source, and rotationally analyzed to yield precise values for the band origins and rotational constants; fluorescence lifetimes were also measured to probe for lifetime lengthening effects due to the RT interaction. The derived A state parameters are compared with previous results for CHF and with predictions of ab initio electronic structure theory. The approach to linearity in the A state is evidenced in a sharp increase in the A rotational constant with bending excitation, and a minimum in the vibrational intervals near 2(9). A fit of the vibrational intervals for the pure bending levels yields an A state barrier to linearity in good agreement both with that previously derived for CHF and ab initio predictions. From the spectra and lifetime measurements, the onset of extensive RT perturbations is found to occur at a higher energy than in CHF, consistent with the smaller A constant. 相似文献
80.
Ghitun M Bonneil E Fortier MH Yin H Killeen K Thibault P 《Journal of separation science》2006,29(11):1539-1549
This work reports on the application of a microfluidic device integrating nanoscale LC to nanoelectrospray MS (nano-LC-chip-MS) for the analysis of complex protein digests. Peak profile analyses of more than 700 peptide ions, reproducibly detected across replicate nano-LC-chip-MS runs (n = 5), indicated that the system provided RSD values of 0.24% on retention time, +/- 30 ppm on m/z measurement and +/- 30% variation on intensity over three orders of magnitude. RP adsorbant media with different alkyl chains and particle size packed in both trapping and separation channels were investigated to improve the chromatographic performance of this system. A two-fold improvement in chromatographic peak capacity was achieved using microfluidic devices comprising a 5 mircrom C3 trap with 2.5 microm C18 trap separation channel compared to the traditional 5 microm C18 stationary phase. Enhanced sample selectivity for the identification of phosphopeptides was obtained by combining immobilized metal affinity media prior to peptide separation on the RP microfluidic device. This system was evaluated in the context of differential phosphoproteome analyses to identify changes in signaling events and protein expression of human monocytes following the administration of phorbol ester. 相似文献