全文获取类型
收费全文 | 60篇 |
免费 | 0篇 |
专业分类
化学 | 51篇 |
力学 | 1篇 |
物理学 | 8篇 |
出版年
2022年 | 1篇 |
2021年 | 2篇 |
2020年 | 5篇 |
2018年 | 3篇 |
2016年 | 1篇 |
2013年 | 3篇 |
2012年 | 3篇 |
2011年 | 2篇 |
2009年 | 1篇 |
2008年 | 3篇 |
2005年 | 3篇 |
2004年 | 3篇 |
2002年 | 5篇 |
2000年 | 1篇 |
1998年 | 2篇 |
1997年 | 1篇 |
1996年 | 1篇 |
1995年 | 1篇 |
1994年 | 1篇 |
1988年 | 1篇 |
1981年 | 3篇 |
1980年 | 4篇 |
1979年 | 2篇 |
1978年 | 1篇 |
1976年 | 1篇 |
1975年 | 1篇 |
1974年 | 2篇 |
1973年 | 1篇 |
1972年 | 1篇 |
1963年 | 1篇 |
排序方式: 共有60条查询结果,搜索用时 41 毫秒
41.
Sudhir Burman Dixit N. Sathyanarayana Augostinos Anagnostopoulos 《Transition Metal Chemistry》1980,5(1):52-55
Summary Ferrous and ferric complexes of 2,4-dithiobiuret (Dtb) of the type Fe(Dtb)m Xn where m, n = 1-3, and X = CI–, Br–, I– and SO
4
2–
, and a neutral Fe(Dtb-H)2 complex have been synthesized and characterised by elemental analyses, magnetic susceptibility, i.r., electronic and Mössbauer spectroscopic studies. From its i.r. spectrum Dtb was found to act as a S,S-coordinating bidentate chelate. The magnetic moment, electronic and Massbauer spectra are consistent with a low spin distorted octahedral structure for the ferric complexes and a high spin form for ferrous complexes. 相似文献
42.
A new technique has been devised to achieve a steady-state polarisation of a stationary electrode with a helical shaft rotating coaxial to it. A simplified theory for the convective hydrodynamics prevalent under these conditions has been formulated. Experimental data are presented to verify the steady-state character of the current-potential curves and the predicted dependence of the limiting current on the rotation speed of the rotor, the bulk concentration of the depolariser and the viscosity of the solution. Promising features of the multiple-segment electrodes concentric to a central disc electrode are pointed out. 相似文献
43.
Palle Swapna Rao D. N. Sathyanarayana 《Journal of polymer science. Part A, Polymer chemistry》2002,40(22):4065-4076
This article describes the results of the preparation and characterization of self‐doped conducting copolymers of aniline and toluidine with m‐aminobenzene sulfonic acid. The copolymers have an intrinsic acid group that is capable of doping polyaniline. Spectroscopic, morphological, and electrical conductivity studies have provided insight into the structural and electronic properties of the copolymers. The differences in the properties of polyaniline and polytoluidine due to the sulfonic acid ring substituent on the phenyl ring are discussed. The scanning electron micrographs of the copolymers reveal regions of sharp‐edged, needle‐shaped structures, whereas the X‐ray diffraction patterns show that the copolymers are relatively more crystalline in nature. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 4065–4076, 2002 相似文献
44.
Vidhika Punjani Dr. Golam Mohiuddin Supreet Kaur Dr. Angshuman Roy Choudhury Dr. Sathyanarayana Paladugu Dr. Surajit Dhara Dr. Sharmistha Ghosh Dr. Santanu Kumar Pal 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(26):5859-5871
Recently, an unprecedented observation of polar order, thermochromic behavior, and exotic mesophases in new chiral, bent-shaped systems with a −CH3 moiety placed at the transverse position of the central core was reported. Herein, a homologous series of compounds with even-numbered carbon chains from n=4 to 18 were synthesized, in which −Cl was substituted for −CH3 at the kink position and a drastic modification in the phase structure of the bent-shaped molecule was observed. An unusual stabilization of the cubic blue phase (BP) over a wide range of 16.4 °C has been witnessed. Two homologues in this series ( 1 -12 and 1 -14) exhibit an interesting phase sequence consisting of BPI/II, chiral nematic, twist grain boundary, smectic A, and smectic X (SmX) phases. The higher homologues ( 1 -16 and 1 -18) stabilize the SmX phase enantiotropically over the entire temperature range. Crystal structure analysis confirmed the bent molecular architecture, with a bent angle of 148°, and revealed the presence of two different molecular conformations in an asymmetric unit of compound 1 -4. A DFT study corroborated that the −Cl moiety at the central core of the molecule led to an increase in the dipole moment along the transverse direction, which, in turn, facilitated the unusual stabilization of frustrated structures. Crystal polymorphism has been evidenced in three homologues ( 1 -10, 1 -12, and 1 -14) of the series. On the application of mechanical pressure through grinding, compound 1 -10 transformed from a bright yellow crystalline solid to a dark orange–green amorphous solid, which reversed upon dropwise addition of dichloromethane, indicating reversible mechanochromism in this class of compounds. In addition, excellent thermochromic behavior has been observed for compound 1 -10 with a controlled temperature–color combination. 相似文献
45.
Girigani Sathyanarayana Singh Harnam Kola Sankar Rao Dayanand Yelmeli Vijayalaxmi Regula Venu Gopal Shah Sakshi Jain Neelu Kumar Pramod 《Research on Chemical Intermediates》2020,46(1):267-281
Research on Chemical Intermediates - A robust and safe industrial process, including five isolations and drying steps for widely prescribed anti-HIV (protease inhibitor) drug darunavir ethanolate... 相似文献
46.
P. Savitha D. N. Sathyanarayana 《Journal of polymer science. Part A, Polymer chemistry》2004,42(17):4300-4310
A series of poly(o‐/m‐toluidine‐co‐o‐/m‐aminoacetophenone) copolymers combining the features of high conductivity and processibility are synthesized and characterized by a number of techniques including 1H NMR; thermogravimetry; IR, Raman, and UV–visible spectroscopy; scanning electron microscopy; and X‐ray diffraction. The copolymers are synthesized by the emulsion and inverse emulsion methods using conventional ammonium persulfate and a new oxidant, benzoyl peroxide, respectively. The influence of the polymerization conditions such as the monomer feed ratios, solvent, and the nonsolvent is investigated. The composition of the resulting copolymers is determined by 1H NMR analysis. The conductivity of the copolymers varies with the aminoacetophenone content in the feed and the polymerization conditions. It is interesting that the conductivity of the copolymers is higher than that of the corresponding homopolymers. The results are rationalized on the basis of the effect of the ? COCH3 substituent on the polymer structure. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4300–4310, 2004 相似文献
47.
Priyadarsi De D. N. Sathyanarayana 《Journal of polymer science. Part A, Polymer chemistry》2002,40(1):9-18
Copolyperoxides of indene and p‐tert‐butylstyrene of different compositions were synthesized by free‐radical‐initiated oxidative copolymerization. The compositions of the copolyperoxides, obtained from 1H and 13C NMR spectra, were used to calculate the reactivity ratios of the monomers. The reactivity ratios indicated a larger proportion of indene units in random placement in the copolyperoxides. Thermal‐degradation studies by differential scanning calorimetry and electron‐impact mass spectrometry supported alternating peroxide units in the copolymer backbone. The activation energy for thermal degradation suggested that the degradation was dependent on the dissociation of the peroxide (? O? O? ) bonds in the backbone of the copolyperoxide chain. The flexibility of the copolyperoxides was examined in terms of the glass‐transition temperature. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 40: 9–18, 2002 相似文献
48.
Arruri Sathyanarayana Shin-ya Nakamura Kyohei Hisano Osamu Tsutsumi Katam Srinivas Ganesan Prabusankar 《中国科学:化学(英文版)》2018,61(8):957-965
Thermally stable, solid-state luminescent organic materials are highly desired for the development of practical applications. Herein we synthesized new gold(I) complexes with N-heterocyclic carbene ligands, which have the ability to form strong metal-organic bond. Consequently, their thermochemical stability is enhanced at temperatures around 300 °C. Precise design of the molecular structure of the ligands, with a focus on ensuring low steric hindrance around Au atoms in order to limit disturbances to Au/Au interactions, provided a complex with a densely packed crystal with a shorter intermolecular Au–Au distance (3.17 Å) than the typical distance. In the solid state, this complex exhibited strong aurophilic interactions, which generated intense phosphorescence even in air at room temperature (quantum yield=16%) in spite of absence of any phosphorescence in solution. This behavior is characteristic for solid-state luminescence referred to as aggregation-controlled emission. Furthermore, the gold (I) complex displays capacity for mechano- and vapo-chromism—that is, the ability to change color reversibly in response to the application of external stimuli. We believe that the proposed design framework, which involves controlling thermal stability and luminescence property separately, provides a new opportunity for the development of practical applications using solid-state luminescent organic molecules. 相似文献
49.
Ulaganathan Sivagnanam Shweta Narayana Murthy Sathyanarayana N. Gummadi 《BMC biochemistry》2016,17(1):10
Background
Human phospholipid scramblase 1 (hPLSCR1) was initially identified as a Ca2+ dependent phospholipid translocator involved in disrupting membrane asymmetry. Recent reports revealed that hPLSCR1 acts as a multifunctional signaling molecule rather than functioning as scramblase. hPLSCR1 is overexpressed in a variety of tumor cells and is known to interact with a number of protein molecules implying diverse functions.Results
In this study, the nuclease activity of recombinant hPLSCR1 and its biochemical properties have been determined. Point mutations were generated to identify the critical region responsible for the nuclease activity. Recombinant hPLSCR1 exhibits Mg2+ dependent nuclease activity with an optimum pH and temperature of 8.5 and 37 °C respectively. Experiments with amino acid modifying reagents revealed that histidine, cysteine and arginine residues were crucial for its function. hPLSCR1 has five histidine residues and point mutations of histidine residues to alanine in hPLSCR1 resulted in 60 % loss in nuclease activity. Thus histidine residues could play a critical role in the nuclease activity of hPLSCR1.Conclusions
This is the first report on the novel nuclease activity of the multi-functional hPLSCR1. hPLSCR1 shows a metal dependent nuclease activity which could play a role in key cellular processes that needs to be further investigated.50.
Sudhir Burman Dixit N. Sathyanarayana Augoustinos Anagnostopoulos 《Transition Metal Chemistry》1979,4(6):364-367
Summary 4,4-Bipyridyl (4,4-bipy) complexes of ferrous salts of the Fe(4,4-bipy)x(anion)y type (where x or y=1 or 2) and of ferric salts of the Fe(4,4-bipy)m(anion)n type (where m=1 or 2 and n=3) have been synthesised. Elemental analyses, i.r. and electronic spectra, magnetic and Mössbauer studies have been performed to characterize the complexes. 4,4-Bipy and some anions are inferred to act as bridging ligands. The magnetic moments, electronic and Mössbauer spectra suggest that the complexes are of high spin type with distorted octahedral structures. The value of the isomer shift and quadrupole splitting are discussed in terms of bonding of the ligand and anions. 相似文献