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91.
A study of the viability of three derivatizing reagents for obtaining amino acid profiles in honey through high performance liquid chromatography (HPLC) is presented. A method using diode array detection based on a reaction with diethyl ethoxymethylene malonate (DEMM) and two other methods using fluorescence detection based on derivatization with fluorenylmethyl chloroformate (FMOC-Cl) and 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate (AQC) have been developed. The three methods yield detection limits close to the ppb level, but vary in relation to other analytical characteristics. The use of methyl chloroformate derivatives allows the profile to be obtained with the greatest sensitivity within a short time frame. On applying such methods to honey samples of diverse botanical origin, we observe that the proline values obtained are always lower than those found using the official spectrophotometric method, thereby underlining the advisability of using HPLC methods to reduce uncertainty in these results. 相似文献
92.
Abstract— Enzyme generated triplet acetone transfers its energy to Chl a to form the first excited singlet of the acceptor, as shown by the suppression of the acetone chemiphosphorescence and concomitant appearance of the Chl fluorescence. 相似文献
93.
The self‐complementary tetrameric propargyl triols 8, 14, 18 , and 21 were synthesized to investigate the duplex formation of self‐complementary, ethynylene‐linked UUAA, AAUU, UAUA, and AUAU analogues with integrated bases and backbone (ONIBs). The linear synthesis is based on repetitive Sonogashira couplings and C‐desilylations (34–72% yield), starting from the monomeric propargyl alcohols 9 and 15 and the iodinated nucleosides 3, 7, 11 , and 13 . Strongly persistent intramolecular H‐bonds from the propargylic OH groups to N(3) of the adenosine units prevent the gg‐type orientation of the ethynyl groups at C(5′). As such, an orientation is required for the formation of cyclic duplexes, this H‐bond prevents the formation of duplexes connected by all four base pairs. However, the central units of the UAUA and AAUU analogues 18 and 14 associate in CDCl3/(D6)DMSO 10 : 1 to form a cyclic duplex characterized by reverse Hoogsteen base pairing. The UUAA tetramer 8 forms a cyclic UU homoduplex, while the AUAU tetramer 21 forms only linear associates. Duplex formation of the O‐silylated UUAA and AAUU tetramers is no longer prevented. The self‐complementary UUAA tetramer 22 forms Watson–Crick‐ and Hoogsteen‐type base‐paired cyclic duplexes more readily than the sequence‐isomeric AAUU tetramer 23 , further illustrating the sequence selectivity of duplex formation. 相似文献
94.
V. Nastro D. Vuono M. Guzzo G. Niceforo I. Bruno P. De
Luca 《Journal of Thermal Analysis and Calorimetry》2006,84(1):181-184
The aim of this paper is to characterize some raw
materials used for ceramics material production. Five samples of clay have
been analyzed. It has been carried out a patterned sampling in a quarry in
Rosarno (South Italy).
Chemical-physical
properties on clay samples are determined. Test pieces have been prepared
and physical properties after firing are determined by DSC thermal analysis,
XRD analysis and X-ray fluorescence. It is important to note the high amount
of Fe2O3. The mixture principally
contains quartz, illite and oligoclase. It has been observed the colour and
the shape after firing: predominant colour is red. In this case the clay has
been used in mixtures covered with glazes. The colour of internal clay is
hidden by opaque of glazes. The analysed raw materials can be used in a slip
for single fired red tiles. The A2sp clay produces best ceramics at 1000°C. 相似文献
95.
96.
97.
98.
Reinoso S Vitoria P Gutiérrez-Zorrilla JM Lezama L San Felices L Beitia JI 《Inorganic chemistry》2005,44(26):9731-9742
Reaction of in situ generated copper(II)-monosubstituted Keggin polyoxometalates and copper(II)-bipyridine-oxalate complexes in the corresponding alkaline acetate buffer led to the formation of hybrid metal organic-inorganic compounds K(2)[{SiW(11)O(39)Cu(H(2)O)}{Cu(2)(bpy)(2)(H(2)O)(2)(mu-ox)}(2)].14H(2)O (1), K(14)[{SiW(11)O(39)Cu(H(2)O)}{Cu(2)(bpy)(2)(mu-ox)}](2)[SiW(11)O(39)Cu(H(2)O)].55H(2)O (2), (NH(4))(4)[{SiW(11)O(39)Cu(H(2)O)}{Cu(2)(bpy)(2)(mu-ox)}].10H(2)O (3), and Rb(4)[{SiW(11)O(39)Cu(H(2)O)}{Cu(2)(bpy)(2)(mu-ox)}].10H(2)O (4). Their structures have been established by single-crystal X-ray diffraction. The main structural feature of these compounds is the presence of copper(II)-monosubstituted alpha-Keggin polyoxoanions as inorganic building blocks, on which the mu-oxalatodicopper metalorganic blocks are supported. Compound 1contains the discrete hybrid polyanion [{SiW(11)O(39)Cu(H(2)O)}{Cu(2)(bpy)(2)(H(2)O)(2)(mu-ox)}(2)](2)(-), whereas the polymeric hybrid polyanion [{SiW(11)O(39)Cu(H(2)O)}{Cu(2)(bpy)(2)(mu-ox)}(2)](n)(4)(n)(-) gives a monodimensional character to compounds 2-4. Magnetic and EPR results are discussed with respect to the crystal structure of the compounds. DFT calculations on both the [Cu(2)(bpy)(2)(H(2)O)(4)(mu-ox)](2+) cationic complex and the metalorganic blocks have been performed in order to determine the optimized geometry and the magnetic coupling constants, respectively. 相似文献
99.
Bruno Cordani 《Communications in Mathematical Physics》1986,103(3):403-413
The manifoldM of null rays through the origin of 2,n+1 is diffeomorphic toS
1×S
n
, and it is a homogeneous space of SO(2,n+1). This group therefore acts onT*M, which we show to be the generating manifold of the extended phase space of the regularized Kepler Problem. A local canonical chart inT*M is found such that the restriction to the subbundle of the null nonvanishing covectors is given byp
0+H(q,p)=0, whereH(q,p) is the Hamiltonian of the Kepler Problem. By means of this construction, we get some results that clarify and complete the previous approaches to the problem. 相似文献
100.
Luis JM Torrent-Sucarrat M Solà M Bishop DM Kirtman B 《The Journal of chemical physics》2005,122(18):184104
Our new simple method for calculating accurate Franck-Condon factors including nondiagonal (i.e., mode-mode) anharmonic coupling is used to simulate the C2H4+X2B3u<--C2H4X1A(g) band in the photoelectron spectrum. An improved vibrational basis set truncation algorithm, which permits very efficient computations, is employed. Because the torsional mode is highly anharmonic it is separated from the other modes and treated exactly. All other modes are treated through the second-order perturbation theory. The perturbation-theory corrections are significant and lead to a good agreement with experiment, although the separability assumption for torsion causes the C2D4 results to be not as good as those for C2H4. A variational formulation to overcome this circumstance, and deal with large anharmonicities in general, is suggested. 相似文献