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1.
Takanari Yasui Takeshi Ohtsuka Tetsu Suzuki Shigeki Okajima Kazuya Nakayama Mitsuru Tomioka Katsuhiro Kamimura Takeo Namekata Hiroaki Minamide Hiromasa Ito 《International Journal of Infrared and Millimeter Waves》2006,27(2):199-210
A new, wide-band, high-speed and high-sensitivity THz detector has been developed. The prototype detector consists of a parabolic
cylindrical mirror, a long wire antenna and a Schottky barrier diode. Direct detection measurements have shown a stable sensitivity
of 150 ± 50 V/W for 1–2 THz without any adjustments. The long wire antenna was fixed at the focus of parabolic cylindrical
mirror then it has been realized less operation steps, easy coupling to the external THz signals and a dramatic enhancement
in the practicality of this system. The optically polished mirror and frosted surface one showed comparable sensitivities,
thus easy polishing and less cost mirror fabrication can be applied for this system. The radiation pattern showed a maximum
radiation angle of approximately 23° with its dominant main lobe, which was attributed to the wire antenna character and confirmed
good agreements with classical antenna theory. 相似文献
2.
In order to calculate the cross sections of the muonic atom-nucleus collisions, we have proposed a precise numerical method, a non-adiabatic coupled-rearrangement-channel method with the use of the Jacobian coordinates for the three-body system in the whole space. The scattering boundary condition is correctly imposed along the coordinates; this method does not suffer from the well known defects of the method of adiabatic representation. We applied our method to the muonic atom-nucleus collisions for an incident c.m. energies of 0.001–100 eV. 相似文献
3.
4.
Tomohiro Ishikawa Yoshiaki Inaki Kiichi Takemoto 《Journal of polymer science. Part A, Polymer chemistry》1980,18(6):1847-1856
Copolymers of L -lysine and L -lysine derivatives which contained nucleic acid bases substituted on the Nε position were synthesized by grafting nucleic acid derivatives onto poly-L -lysine. The conformation and interaction of these copolymers in solution were studied by using spectroscopic measurements. They existed in helical conformation at neutral pH values, and the polymer complex formation among them was examined by ultraviolet (UV) measurements in organic solvents. A decrease in the nucleic acid base content of the copolymers resulted in a decrease in helical structures and also in interactions with the polymer-containing complementary bases. 相似文献
5.
Takashi Kamimura Tsukio Masegi Mitsuo Sekine Tsujiaki Hata 《Tetrahedron letters》1984,25(38):4241-4244
Diisopropylethylamine was effective as a base for acylation of 2′,3′,5′-tri-O-acetyluridine with various acid chlorides. The 13C NMR spectra of the products and related compounds showed clearly that the acyl groups intoduced to the uracil moiety are attached to the N3-nitrogen. 相似文献
6.
We calculated the (dµ)
n=1 +t scattering in the energy region of the (dtµ)* resonant states below then=2 level of the tµ atom. From the cross sections, we estimated the resonant energies, widths and branching ratios. We found eleven resonant states with angular momentumJ=0, and some of their resonant energies relative to then=2 level of tµ are small enough to form the [(dtµ)* dee] by the Vesman mechanism. These resonant states decay to (dµ)[inn=1 +t or (tµ)
n=1 + d scattering states. The total decay rates are about 1011 s–1 which is three orders of magnitude larger than the fusion rates of (dtµ)*4 He + n+ 17.6 MeV + µ. The main part of the decaying channel from the shallow resonant states is the (dµ)
n=1 +t channel. The branching ratios of the (dµ)
n=1 +t decay channel are around 0.9. Most of the muons that reach to then=2 states of tµ can transfer to then=1 state of du through (tµ)
n=2 + D2 [(dtµ)*dee] and (dtµ)* (dµ)
n=1 +t processes. 相似文献
7.
Using the coupled rearrangement channel method, we have calculated resonance energies for meta-stable states of the molecular ion dtµ* associated with the adiabatic 3 potential. The vacuum polarization effect was taken into account by direct inclusion of the Uehling potential in our three-body Hamiltonian. Comparing with the solution of the pure Coulombic Schrödinger equation a shift of approximately +0.1 eV is found. Thus the infinite series of states of the Coulombic Schrödinger equation becomes truncated. Eleven states remain semi-bound, five of them with binding energy smaller than the dissociation energy of the D2 molecule, facilitating formation of dtµ* in tµ(2s)-D2 scattering by means of the Vesman-mechanism. 相似文献
8.
Hiromori Tsutsumi Ken Okanishi Mikiji Miyata Kiichi Takemoto 《Journal of polymer science. Part A, Polymer chemistry》1990,28(6):1527-1538
Inclusion polymerization of 1-chlorobutadiene was studied using 3α,12α-dihydroxy-5β-cholan-24-oic acid (deoxycholic acid, DCA) as host molecules. It was found that the poly(1-chlorobutadiene) had almost 100% of head to tail, trans-1,4-structure on the basis of 13C-NMR and IR spectroscopies. This was the first example of preparing the highly regulated poly(1-chlorobutadiene) by using the inclusion polymerization technique. The polymers obtained were optically active and the maximum value of specific rotation was [α]D-41.9°. Both the rate constants and the value of activation energy of the elementary reactions of inclusion polymerization of 1-chlorobutadiene were determined by graphical evaluation. The activation energy of propagation and termination was 11.7 and 11.1 kcal/mol, respectively. 相似文献
9.
Yoshiaki Inaki Hidekazu Futagawa Kiichi Takemoto 《Journal of polymer science. Part A, Polymer chemistry》1980,18(10):2959-2969
Cyclic derivatives of uracil and thymine were synthesized from their corresponding 1-(2′-chloroethyl) derivatives by dehydrochlorination. These compounds were found to undergo a variety of reactions, giving many valuable derivatives of uracil and thymine. The cyclic derivatives, as monomers, were polymerized with a cationic initiator by a unique ring-opening process. The polymerization proceeded by ring opening with isomerization of the pyrimidine ring to give a polymer in which pyrimidine rings were connected with ethylene between N-1 and N-3 or O-4 in the pyrimidine ring. The structure of these polymers was determined by nuclear magnetic resonance (NMR), ultraviolet (UV), infrared (IR), and mass spectra. The structure was affected by polymerization temperature. 相似文献
10.
Akio Kamimura Rie MoritaKenji Matsuura Hiromasa MitsuderaMasashi Shirai 《Tetrahedron》2003,59(50):9931-9938
A convenient stereoselective synthesis of β-lactams from thio-Michael/aldol tandem adduct is described. syn-Selective tandem reaction followed by amidation and intramolecular SN2 reaction provided β-lactams in diastereomerically pure form. The tandem reaction with aliphatic aldehydes, on the other hand, afforded a mixture of diastereomers of corresponding tandem adducts in about 3:1 ratio so that the conversion to β-lactams afforded a diastereomeric mixture. As an alternative approach to prepare the tandem adducts, the stereoselective Michael addition of aliphatic thiols to Baylis-Hillman adduct was developed. The stereoselectivity was sensitive to the protective group at the hydroxyl group and TBS protection brought the most successful syn-selective formation of the tandem adducts. The procedure could be applied to the ketone derivatives of the Baylis-Hillman adduct but no selectivity was observed for the nitrile-Baylis-Hillman adducts. A similar conversion of the adduct provided desired β-lactams stereoselectively. 相似文献