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1.
Saleh Al-Omari Nawash Alghezawi Mousa Al-Noaimi Akram Aqili Ibrahim F. Al-Hamarneh Mohammad Marashdeh 《Journal of fluorescence》2014,24(3):835-839
The shift of the Q-band of sodium zinc(II)-2,9,16,23-phthalocyanine tetracarboxylate (ZnPc(COONa)4) to about 800 nm is attributed to the influence of the electron-donating property of the carboxylate groups substituted in the β–position. ZnPc(COONa)4 which was found to have a symmetry of D 2h characterized by a splitting of the Q transition. This splitting was interpreted by the formation of dianionic symmetric ZnPc(COONa)4 resulting from the dissociation of the pyrrole protons as well as the possibility of Na+ dissolution of ZnPc(COONa)4 in the aqueous solution of NaOH. 相似文献
2.
B. A. Howell H. Dangalle M. Al-Omari 《Journal of Thermal Analysis and Calorimetry》2011,106(1):129-137
A difunctional imide monomer may be produced from 4-nitrophthalic anhydride and m-phenylenediamine. The requisite anhydride may be generated by nitration of phthalimide followed by hydrolysis to the corresponding
acid and dehydration. All intermediate compounds have been fully characterized using spectroscopic and thermal methods. 相似文献
3.
Elzain M. Al Rawas A. Yousif A. Gismelseed A. Rais A. Al-Omari I. Bouziane K. Widatallah H. 《Hyperfine Interactions》2004,158(1-4):205-209
Time differential perturbed γ-γ angular correlation technique was used to measure the magnetic hyperfine field (MHF) at Tb
sites in the intermetallic compound Tb3In5 using the 140La → 140Ce nuclear probe. The measurements were carried out in the temperature range of 8 to 295 K. Two different temperature dependent
magnetic frequencies were observed below 30 K, which were assigned as 140Ce substituting the two inequivalent Tb sites in the orthorhombic structure of Tb3In5. The temperature dependence of MHF also shows a possible deviation from an expected Brillouin-like behavior for temperatures
below 18 K. A Néel transition at 27 K was observed from magnetization measurements in the samples. The magnetization as a
function of the applied magnetic field was measured at two temperatures, 5 and 40 K, and the results show antiferromagnetic
and a typical paramagnetic behavior, respectively. In both cases it was not observed saturation under high magnetic field. 相似文献
4.
Kamzin A. S. Obaidat I. M. Valliulin A. A. Semenov V. G. Al-Omari I. A. 《Physics of the Solid State》2020,62(10):1933-1943
Physics of the Solid State - The magnetic structure and the composition of Fe3O4/γ-Fe2O3 nanoparticles are studied at 300 and 80 K with Mössbauer spectroscopy. We found that the... 相似文献
5.
Omar K. Jaradat Ahmad Al-Omari Shaher Momani 《Nonlinear Analysis: Theory, Methods & Applications》2008
In this paper we will study the existence and uniqueness of mild solution for the semilinear initial value problem of non-integer order:
where, α∈(0,1] and f(t,u(t),Gu(t),Su(t)) is a given function. 相似文献
u(α)(t)=Au(t)+f(t,u(t),Gu(t),Su(t)),
6.
MF Miller IA Franchi AS Sexton CT Pillinger 《Rapid communications in mass spectrometry : RCM》1999,13(13):1211-1217
The use of infrared laser-assisted fluorination to release oxygen from milligram quantities of silicates or other oxide mineral grains is a well-established technique. However, relatively few studies have reported the optimisation of this procedure for oxygen-17 isotope measurements. We describe here details of an analytical system using infrared (10 μm) laser-assisted fluorination, in conjunction with a dual inlet mass spectrometer of high resolving power ( approximately 250) to provide (17)O and (18)O oxygen isotope measurements from 0.5-2 mg of silicates or other oxide mineral grains. Respective precisions (1) of typically 0.08 and 0.04 per thousand are obtained for the complete analytical procedure. Departures from the mass-dependent oxygen isotope fractionation line are quantified by Delta(17)O; our precision (1) of such measurements on individual samples is shown to be +/-0.024 per thousand. In turn, this permits the offset between parallel, mass-dependent fractionation lines to be characterised to substantially greater precision than has been possible hitherto. Application of this system to investigate the (17)O versus (18)O relationship for numerous terrestrial whole-rock and mineral samples, of diverse geological origins and age, indicates that the complete data set may be described by a single, mass-dependent fractionation line of slope 0.5244+/- 0.00038 (standard error). Copyright 1999 John Wiley & Sons, Ltd. 相似文献
7.
Shongwe MS Al-Rahbi SH Al-Azani MA Al-Muharbi AA Al-Mjeni F Matoga D Gismelseed A Al-Omari IA Yousif A Adams H Morris MJ Mikuriya M 《Dalton transactions (Cambridge, England : 2003)》2012,41(8):2500-2514
The two potentially tridentate and monoprotic Schiff bases acetylpyridine benzoylhydrazone (HL(1)) and acetylpyridine 4-tert-butylbenzoylhydrazone (HL(2)) demonstrate remarkable coordination versatility towards iron on account of their propensity to undergo tautomeric transformations as imposed by the metal centre. Each of the pyridyl aroylhydrazone ligands complexes with the ferrous or ferric ion under strictly controlled reaction conditions to afford three six-coordinate mononuclear compounds [Fe(II)(HL)(2)](ClO(4))(2), [Fe(II)L(2)] and [Fe(III)L(2)]ClO(4) (HL = HL(1) or HL(2)) displaying distinct colours congruent with their intense CT visible absorptions. The synthetic manoeuvres rely crucially on the stoichiometry of the reactants, the basicities of the reaction mixtures and the choice of solvent. Electrochemically, each of these iron compounds exhibits a reversible metal-centred redox process. By all appearances, [Fe(III)(L(1))(2)]ClO(4) is one of only two examples of a crystallographically elucidated iron(III) bis-chelate compound of a pyridyl aroylhydrazone. Several pertinent physical measurements have established that each of the Schiff bases stabilises multiple spin states of iron; the enolate form of these ligands exhibits greater field strength than does the corresponding neutral keto tautomer. To the best of our knowledge, [Fe(III)(L(1))(2)]ClO(4) and [Fe(III)(L(2))(2)]ClO(4) are the first examples of ferric spin crossovers of aroylhydrazones. Whereas in the former the spin crossover (SCO) is an intricate gradual process, in the latter the (6)A(1)?(2)T(2) transition curve is sigmoidal with T(?)~280 K and the SCO is virtually complete. As regards [Fe(III)(L(1))(2)]ClO(4), M?ssbauer and EPR spectroscopic techniques have revealed remarkable dependence of the spin transition on sample type and extent of solvation. In frozen MeOH solution at liquid nitrogen temperature, both iron(III) compounds exist wholly in the doublet ground state. 相似文献
8.
MS Shongwe UA Al-Zaabi F Al-Mjeni CS Eribal E Sinn IA Al-Omari HH Hamdeh D Matoga H Adams MJ Morris AL Rheingold E Bill DJ Sellmyer 《Inorganic chemistry》2012,51(15):8241-8253
Several potentially tridentate pyridyl and phenolic Schiff bases (apRen and HhapRen, respectively) were derived from the condensation reactions of 2-acetylpyridine (ap) and 2'-hydroxyacetophenone (Hhap), respectively, with N-R-ethylenediamine (RNHCH(2)CH(2)NH(2), Ren; R = H, Me or Et) and complexed in situ with iron(II) or iron(III), as dictated by the nature of the ligand donor set, to generate the six-coordinate iron compounds [Fe(II)(apRen)(2)]X(2) (R = H, Me; X(-) = ClO(4)(-), BPh(4)(-), PF(6)(-)) and [Fe(III)(hapRen)(2)]X (R = Me, Et; X(-) = ClO(4)(-), BPh(4)(-)). Single-crystal X-ray analyses of [Fe(II)(apRen)(2)](ClO(4))(2) (R = H, Me) revealed a pseudo-octahedral geometry about the ferrous ion with the Fe(II)-N bond distances (1.896-2.041 ?) pointing to the (1)A(1) (d(π)(6)) ground state; the existence of this spin state was corroborated by magnetic susceptibility measurements and M?ssbauer spectroscopy. In contrast, the X-ray structure of the phenolate complex [Fe(III)(hapMen)(2)]ClO(4), determined at 100 K, demonstrated stabilization of the ferric state; the compression of the coordinate bonds at the metal center is in accord with the (2)T(2) (d(π)(5)) ground state. Magnetic susceptibility measurements along with EPR and M?ssbauer spectroscopic techniques have shown that the iron(III) complexes are spin-crossover (SCO) materials. The spin transition within the [Fe(III)N(4)O(2)](+) chromophore was modulated with alkyl substituents to afford two-step and one-step (6)A(1) ? (2)T(2) transformations in [Fe(III)(hapMen)(2)]ClO(4) and [Fe(III)(hapEen)(2)]ClO(4), respectively. Previously, none of the X-salRen- and X-sal(2)trien-based ferric spin-crossover compounds exhibited a stepwise transition. The optical spectra of the LS iron(II) and SCO iron(III) complexes display intense d(π) → p(π)* and p(π) → d(π) CT visible absorptions, respectively, which account for the spectacular color differences. All the complexes are redox-active; as expected, the one-electron oxidative process in the divalent compounds occurs at higher redox potentials than does the reverse process in the trivalent compounds. The cyclic voltammograms of the latter compounds reveal irreversible electrochemical generation of the phenoxyl radical. Finally, the H(2)salen-type quadridentate ketimine H(2)hapen complexed with an equivalent amount of iron(III) to afford the μ-oxo-monobridged dinuclear complex [{Fe(III)(hapen)}(2)(μ-O)] exhibiting a distorted square-pyramidal geometry at the metal centers and considerable antiferromagnetic coupling of spins (J ≈ -99 cm(-1)). 相似文献
9.
Kamzin A. S. Obaidat I. M. Valliulin A. A. Semenov V. G. Al-Omari I. A. 《Physics of the Solid State》2020,62(11):2167-2172
Physics of the Solid State - The composition and the magnetic structure of Fe3O4/γ-Fe2O3 nanoparticles placed into external magnetic field with a strength of 1.8 kOe are studied with... 相似文献
10.