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81.
S.?Dey S.S.?Dasgupta C.C.?Dey P.?Bhattacharya 《The European Physical Journal A - Hadrons and Nuclei》2003,16(2):193-197
A kinematically complete experiment has been performed to study the α-n final-state interaction (FSI) in the α + d ↦α + p
+ n break-up reaction at 50 MeV incident energy for the alpha-particles. For this, we have chosen four pairs of correlation
angles for the outgoing alpha and protons. These are ( θα = 18°, θp = 42°), ( θα = 20°, θp = 45°), ( θα = 22°, θp = 42°) and ( θα = 22°, θp = 47°), selected kinematically where the allowed phase spaces are in favor of the α-n final-state interaction. Our experimental
data show strong α-n FSI in all the selected configurations. Also, the FSI is found to be stronger at the lower alpha-particle
energy when two FSI peaks appear in the same configuration.
Received: 17 June 2002 / Accepted: 3 October 2002 / Published online: 4 February 2003
RID="a"
ID="a"e-mail: dey_s2001@yahoo.com; Present address: 445 Waupelani Drive, Apt. F3, State College, PA 16801, USA.
Communicated by M. Gar?on 相似文献
82.
Dipsikha Bhattacharya Sumanta K. Sahu Indranil Banerjee Manasmita Das Debashish Mishra Tapas K. Maiti Panchanan Pramanik 《Journal of nanoparticle research》2011,13(9):4173-4188
In this article, we report the design and synthesis of a series of well-dispersed superparamagnetic iron oxide nanoparticles
(SPIONs) using chitosan as a surface modifying agent to develop a potential T
2 contrast probe for magnetic resonance imaging (MRI). The amine, carboxyl, hydroxyl, and thiol functionalities were introduced
on chitosan-coated magnetic probe via simple reactions with small reactive organic molecules to afford a series of biofunctionalized
nanoparticles. Physico-chemical characterizations of these functionalized nanoparticles were performed by TEM, XRD, DLS, FTIR,
and VSM. The colloidal stability of these functionalized iron oxide nanoparticles was investigated in presence of phosphate
buffer saline, high salt concentrations and different cell media for 1 week. MRI analysis of human cervical carcinoma (HeLa)
cell lines treated with nanoparticles elucidated that the amine-functionalized nanoparticles exhibited higher amount of signal
darkening and lower T
2 relaxation in comparison to the others. The cellular internalization efficacy of these functionalized SPIONs was also investigated
with HeLa cancer cell line by magnetically activated cell sorting (MACS) and fluorescence microscopy and results established
selectively higher internalization efficacy of amine-functionalized nanoparticles to cancer cells. These positive attributes
demonstrated that these nanoconjugates can be used as a promising platform for further in vitro and in vivo biological evaluations. 相似文献
83.
A. Bhattacharya 《Journal of Thermal Analysis and Calorimetry》1997,49(3):1365-1371
Aesthetic and utilitarian properties of traditional ceramic wares as well as engineering properties of modern advanced ceramics are attained by maintaining an optimum temperature-time-atmosphere relationship, called firing schedule, in the kiln. The contribution of modern thermal analysis (TA) techniques such as TG/DTG, TG/EGA, TG/MS, DTA, DSC, TDA, etc. in 1) optimizing production steps by raw material quality control, by studying binder burn out, product densification, 2) in simulating appropriate preheating, firing and cooling schedules as well as 3) in developing shorter firing cycles has been extensively reported in recent literature. The paper will first discuss theoretical curves and energy required for ceramic firing and present from the literature selected examples of applications of thermal analysis in ceramic technology. 相似文献
84.
Letd>1, and letα andβ be mixing ? d -actions by automorphisms of zero-dimensional compact abelian groupsX andY, respectively. By analyzing the homoclinic groups of certain sub-actions ofα andβ we prove that, if the restriction ofα to some subgroup Γ ? ? d of infinite index is expansive and has completely positive entropy, then every measurable factor mapφ: (X, α)→(Y, β) is almost everywhere equal to an affine map. The hypotheses of this result are automatically satisfied if the actionα contains an expansive automorphismα n ,n ∈ ? d , or ifα arises from a nonzero prime ideal in the ring of Laurent polynomials ind variables with coefficients in a finite prime field. Both these corollaries generalize the main theorem in [9]. In several examples we show that this kind of isomorphism rigidity breaks down if our hypotheses are weakened. 相似文献
85.
Tiwari AD Mishra AK Mishra SB Mamba BB Maji B Bhattacharya S 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,79(5):1050-1056
The thiocarbohydrazone Schiff-base ligand with a nitrogen and sulphur donor was synthesized through condensation of pyridine-2-carbaldehyde and thiocarbohydrazide. Schiff-base ligands have the ability to conjugate with metal salts. A series of metal complexes with a general formula [MCl2(H2L)]·nH2O (MNi, Co, Cu and Zn) were synthesized by forming complexes of the N1,N5-bis[pyridine-2-methylene]-thiocarbohydrazone (H2L) Schiff-base ligand. These metal complexes and ligand were characterized by using ultraviolet-visible (UV-Vis), Fourier Transform Infrared (FT-IR), 1H and 13C NMR spectroscopy and mass spectroscopy, physicochemical characterization, CHNS and conductivity. The biological activity of the synthesized ligand was investigated by using Escherichia coli DNA as target. The DNA interaction of the synthesized ligand and complexes on E. coli plasmid DNA was investigated in the aqueous medium by UV-Vis spectroscopy and the binding constant (Kb) was calculated. The DNA binding studies showed that the metal complexes had an improved interaction due to trans-geometrical isomers of the complexes than ligand isomers in cis-positions. 相似文献
86.
Arsenic(III) sorption on nanostructured cerium incorporated manganese oxide (NCMO): a physical insight into the mechanistic pathway 总被引:1,自引:0,他引:1
Gupta K Bhattacharya S Nandi D Dhar A Maity A Mukhopadhyay A Chattopadhyay DJ Ray NR Sen P Ghosh UC 《Journal of colloid and interface science》2012,377(1):269-276
Arsenic(III) sorption was investigated with nanostructured cerium incorporated manganese oxide (NCMO). The pH between 6.0 and 8.0 was optimized for the arsenic(III) sorption. Kinetics and equilibrium data (pH=7.0±0.2, T=303±1.6 K, and I=0.01 M) of arsenic(III) sorption by NCMO described, respectively, the pseudo-second order and the Freundlich isotherm equations well. The sorption process was somewhat complicated in nature and divided into two different segments, initially very fast sorption followed by slow intraparticle diffusion process. Sorption reaction of arsenic(III) on NCMO was endothermic (ΔH°=+13.46 kJ mol(-1)) and spontaneous (ΔG°=-24.75 to -30.15 kJ mol(-1) at T=283-323 K), which took place with increasing entropy (ΔS°=+0.14 kJ mol(-1)K(-1)) at solid-liquid interface. Energy of arsenic(III) sorption estimated by analyzing the equilibrium data using the D-R isotherm model was 15.4 kJ mol(-1), indicating the ion-exchange type mechanism. Raman, FT-IR, pH effect, desorption, etc. studies indicated that arsenic(III) was oxidized to arsenic(V) during the sorption process. 相似文献
87.
Halder A Bhatt S Nayak SK Chattopadhyay S Bhattacharya S 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,84(1):25-31
The present article reports the spectroscopic investigations on non-covalent interaction of fullerenes C(60) and C(70) with a macrocyclic receptor molecule, namely, 1,3,5,7-tetrahomo-p-tert-butylcalix[8]arene (1) in toluene. Jobs method of continuous variation reveals 1:1 stoichiometry for the fullerene complexes of 1. The most fascinating feature of the present study is that 1 binds selectively C(60) compared to C(70) as obtained from binding constant (K) data of C(60)-1 (K(C60-1)) and C(70)-1 (K(C70-1)) complexes which are enumerated to be 265,000 dm(3) mol(-1) and 63,43 dm(3) mol(-1), respectively, and selectivity in binding (K(C60-1)/K(C70-1)) is estimated to be 4.18 as obtained from UV-Vis study. Steady state fluorescence studies reveal quenching of fluorescence of 1 in presence of fullerenes and the K value of the C(60)-1 and C(70)-1 complexes are estimated to be 80,760 and 68,780 dm(3) mol(-1), respectively, with selectivity in binding (K(C60-1)/K(C70-1)) ~1.18. (1)H NMR analysis provides very good support in favor of strong binding between C(60) and 1. The high value of K value for C(60)-1 complex indicates that 1 forms an inclusion complex with C(60). 相似文献
88.
Apurba Bhattacharya Nitin C. Patel Ritesh Tichkule Jiejun Wu 《Tetrahedron letters》2006,47(4):565-567
A simple, surfactant-mediated, one-pot, solvent-free dealkylative cleavage of aryl ethers and esters followed by subsequent optional trans-alkylation under essentially neutral conditions has been developed. 相似文献
89.
Santanu Bhattacharya Basudeb Saha Amitava Dutta Pradyot Banerjee 《Coordination chemistry reviews》1998,170(1):47-74
This review narrates the electron transfer reactions of various nickel(III) and nickel(IV) complexes reported during the period 1981 until today. The reactions have been categorized mainly with respect to the type of nickel complexes. The reactivity of nickel(III) complexes of macrocycles, 2,2′-bipyridyl and 1,10-phenanthroline, peptides and oxime–imine, and of nickel(IV) complexes derived from oxime–imine, oxime and miscellaneous ligands with various organic and inorganic electron donors have been included. Kinetic and mechanistic features associated with such interactions have been duly analyzed. The relevance of Marcus cross-relation equations in the delineation of the electron transfer paths has also been critically discussed. 相似文献
90.
Priya Budhani Sayed Aftab Iqbal Suman Malik Mamta Bhattacharya Liviu Mitu 《Journal of Saudi Chemical Society》2010,14(3):281-285
The present paper deals with the synthesis and characterization of Schiff base complexes of pyrazinamide an antitubercular drug. Metals selected for complexation are copper, silver, gold, zinc, mercury, iron and cobalt. The complexes have been suitably synthesized and isolated in pure powdered form. Analytical data agrees with the compositions M(L), M′(L)2 and M″(L)2·2H2O, respectively where M = Ag, M′ = Cu, Au, Zn and Hg and M″ = Fe and Co, ligand metal ratios were also confirmed by monovariation method and Job’s method of continuous variation. Molar conductance values suggest the non ionic nature of the complexes. The tentative structure assigned to the complexes on the basis of stoichiometry and analytical data were further supported by spectral studies viz; IR, NMR, magnetic susceptibility and electronic spectra. A preliminary attempt has also been made to compare the potencies of metal complexes with parent drug. The Cu and Ag complexes are giving encouraging results. Particle size studies further suggest that the drug molecule undergoes reduction in size on complexation. 相似文献