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1.
The spin-1 Ising model with the nearest-neighbour bilinear and biquadratic interactions and single-ion anisotropy is simulated
on a cellular automaton which improved from the Creutz cellular automaton (CCA) for a simple cubic lattice. The simulations
have been made for several k=K/J and d=D/J in the 0≤d<3 and −2≤k≤0 parameter regions. We confirm the existence of the re-entrant and the successive re-entrant phase transitions near the
phase boundary. The phase diagrams characterizing phase transitions are presented for comparison with those obtained from
other calculations. The static critical exponents are estimated within the framework of the finite-size scaling theory at
d=0, 1 and 2 in the interval −2≤k≤0. The results are compatible with the universal Ising critical behavior. 相似文献
2.
3.
Yasemin Oztekin Zafer Yazicigil Ali Osman Solak Zafer Ustundag Zeynel Kilic Selen Bilge 《Surface and interface analysis : SIA》2011,43(5):923-930
Modification of glassy carbon (GC) surfaces with phenanthroline derivatives (PDs) such as 5‐amino‐1,10‐phenanthroline (5AP) and 5,6‐diamino‐1,10‐phenanthroline (56DAP) is described in this study. Surface modification experiments were performed by cyclic voltammetry (CV) scanning from + 1.2 to + 2.7 V at scan rate of 100 mV/s applying 30 potential scans in acetonitrile (CH3CN) containing 1 mM PDs and 100 mM tetrabutylammoniumtetrafluoroborate (TBATFB). The presence of PDs on GC electrode was confirmed using CV, electrochemical impedance spectroscopy (EIS), contact angle measurements and ellipsometry and comparing with the results of bare GC electrode. A mechanism was proposed for the electrochemical modification of the GC electrode surface with PDs. The structure of the 5AP and 56DAP films was also discussed in the light of electrochemical and spectroscopic data. The complex‐forming ability of the modified surfaces against metal cations was investigated by square‐wave voltammetry (SWV). It was shown that surfaces having 1,10‐phenanthroline ligands with different functional groups were quite useful for the determination of transition metal ions. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
4.
The electrochemical behavior of some podands at a benzo[c]cinnoline modified glassy carbon electrode
Aybüke A. ?sb?r Zafer Üstünda? Selen B?lge Amgalan Natsagdorj Emine Kiliç Zeynel Kiliç 《Analytica chimica acta》2005,547(1):59-63
This paper describes the grafting of benzo[c]cinnoline (BCC) molecules on glassy carbon (GC) electrode surface. The attachment of BCC molecules to carbon substrate is induced by the electrochemical reduction of the corresponding diazonium salt. The modification of GC with BCC diazonium salt was done in aprotic solution and proved by blocking of dopamine electron transfer. The presence of BCC at the GC surface was characterized by cyclic voltammetry and X-ray photoelectron spectroscopy (XPS). On modified surface, the electrochemical behavior of two different types of podands and the catalytic effects of the GC-BCC surface were studied. The XPS was used to monitor element characteristics of the adsorbates on the GC surface and confirm the attachment of BCC molecules to the GC surface. 相似文献
5.
Adem Kili Saliha Bege Bekir etinkaya Tuncer Hkelek Zeynel Kili Necla Gündüz Mustafa Yildiz 《Heteroatom Chemistry》1996,7(4):249-256
Reactions of hexachlorocyclotriphosphazatriene, N3P3Cl6 1 , with sodium aryloxides have been studied. Compound 1 was found to react by the nucleophilic substitution pathway to yield monocyclophosphazenes [N3P3Cl6(OC6H2Bu13-2,4,6) 5 and N3P3Cl4(OC6H2Me-4-Bu12-2,6)2 6 ] and bi(cyclophosphazenes) ([Cl5N3P3-P3N3Cl4(OC6H3Bu12-2,6)] 7 and [N3P3(OC6H3Bu12-2,6)5]2 8 ). The unusual bi(cyclophosphazenes) 7 and 8 are the first examples of two cyclotriphosphazene rings linked by a P(SINGLE BOND)P bond [2.193 (2) Å], which have been obtained by reacting 1 with ArONa. The structures of compounds 5–8 are ascertained by elemental analyses, 1H-, 31P-13C-NMR, IR, and MS spectra. The molecular structure of monocyclic-phosphazene 5 was determined by X-ray diffraction techniques for further structural assignment. It crystallizes in the monoclinic space group P21/m with a = 6.144(2), b = 17.079(9), c = 13.181(9) Å, β = 92.79(7), and Z = 2, R = 0.074. Compound 5 is on a crystallographic mirror plane, and there is only a half molecule in the asymmetric unit. © 1996 John Wiley & Sons, Inc. 相似文献
6.
4,4,6,6‐Tetrachloro‐2,2‐(ethylenedioxydi‐o‐phenylenediimino)‐2λ5,4λ5,6λ5‐cyclotriphosphazene
Nagihan aylak Tuncer Hkelek Selen Bilge Bilgehan
zgü Zeynel Kl 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(7):o461-o463
The title ligand, C14H14Cl4N5O2P3, is a cyclophosphazene lariat (PNP pivot) ether with a spiro‐cyclic 11‐membered macrocyclic ring containing two ether O and two N atoms; the phosphazene ring is nearly planar. The macrocyclic ring contains a four‐centred (trifurcate) N—H⋯O/N—H⋯N hydrogen bond, and the relative inner‐hole size of the macrocycle is ∼1.14 Å in radius. The molecules are linked about inversion centres by N—H⋯N hydrogen bonds into centrosymmetric dimers. 相似文献
7.
Phosphorus‐nitrogen compounds. Part 39. Syntheses and Langmuir‐Blodgett thin films and antimicrobial activities of N/N and N/O spirocyclotriphosphazenes with monoferrocenyl pendant arm 下载免费PDF全文
Nuran Asmafiliz Mehmet Civan Arda Özben Zeynel Kılıç Nagehan Ramazanoğlu Leyla Açık Tuncer Hökelek 《应用有机金属化学》2018,32(4)
The Cl substitution reactions of the N/N ( 1 ‐ 3 ) and N/O ( 4 and 5 ) spirocyclic monoferrocenylphosphazenes with 1,4‐dioxa‐8‐azaspiro[4,5]decane (DASD) produce the mono‐ ( 1a ‐ 5a ), geminal‐ ( 1b ‐ 5b ) and tetrakis‐DASD‐substituted ferrocenylspirocyclotriphosphazenes ( 1c ‐ 5c ). The mono‐ and geminal‐DASD‐substituted phosphazenes have two and one stereogenic P‐centers, respectively. The structures of the compounds were established by spectroscopic techniques. The molecular structures of 3a and 2b were evaluated using X‐ray crystallography. Additionally, the ultrathin and highly ordered Langmuir‐Blodgett (LB) films of 3a and 2b were also prepared. The characterizations of the LB films were done using p‐polarized grazing angle (GAIR) and horizontal attenuated total reflectance (HATR) techniques. On the other hand, the antimicrobial activities of the eight phosphazene derivatives against G(+) and G(‐) bacteria and fungi were investigated. Furthermore, the interactions between the compounds and plasmid DNA were studied by agarose gel electrophoresis. 相似文献
8.
Zeynel Abidin Ozdemir 《Physica A》2009,388(12):2461-2468
This paper aims to analyze the linkages between international stock markets and to search for an optimum model for analyzing their interactions taking into consideration their geographical location, using the vector fractionally integrated autoregressive moving-average (VARFIMA) model. This model has not so far been employed in examining the interdependence among the stock markets of Germany, Japan, the UK, and the USA. The results of the paper show that there is an interconnection among the stock markets of these countries. 相似文献
9.
Muhammet I
klan Zeynel Kl Nurcan Akduran Tuncer Hkelek 《Journal of Molecular Structure》2003,660(1-3):167-179
The reactions of 2-trans-6-N4P4(NHPrn)2Cl6 (2), which was obtained from N4P4Cl8 (1) and n-propylamine, with pyrrolidine and t-butylamine in different solvents have been studied. Compound (2) gave two different products, namely monocyclic (3 and 5) and bicyclic (4 and 6) phosphazenes. Compounds (2–6) have been characterized by elemental analysis, IR, 1H-, 13C-, 31P NMR, HETCOR and MS and the structure of compound (5) has been examined crystallographically. The bicyclic phosphazene (6) is the first exciting example of bicyclic phosphazenes containing chlorine atoms, in the literature. The formation mechanisms of bicyclic phosphazenes are re-considered by taking into account the synthesis of compound (6), which contains three stereogenic phosphorus atoms. Compound (5) crystallizes in the monocyclic space group P21/n with a=13.974(2), b=17.836(5), and c=18.683(4) Å, β=98.50(1)°, V=4605.4(2) Å3, Z=4 and Dx=1.051 g cm−3. It consists of a non-centrosymmetric, non-planar phosphazene ring in a saddle conformation, with two n-propylamino (in 2-trans-6 positions) and six bulky t-butylamino side groups. The bulky substituents are instrumental in determining the molecular geometry. 相似文献
10.
The Blume-Emery-Griffiths model is simulated using the cooling algorithm which is improved from the Creutz cellular automaton
(CCA) under periodic boundary conditions. The simulations are carried out on a simple cubic lattice at K/J = −1.5 in the range of −3.5 < D/J < 0.5, with J and K representing the nearestneighbour bilinear and biquadratic interactions, D being the single-ion anisotropy parameter. The
phase diagram characterizing phase transition of the model is obtained. We found different kinds of phase transitions between
the ferromagnetic, quadrupolar, staggered quadrupolar and ferrimagnetic phases for K/J = −1.5. In particular, the region of the phase diagram containing a ferrimagnetic phase is explored and compared to those
obtained by other methods. The simulations confirm that the ferrimagnetic phase occurs in the narrow interval −3.006 ≤ D/J < −3. This result is in a good agreement with Monte Carlo renormalization group and closer to the cluster variation method
result than the mean field approximation result.
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