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1.
A triangulation of a connected closed surface is called weakly regular if the action of its automorphism group on its vertices
is transitive. A triangulation of a connected closed surface is called degree-regular if each of its vertices have the same
degree. Clearly, a weakly regular triangulation is degree-regular. In [8], Lutz has classified all the weakly regular triangulations
on at most 15 vertices. In [5], Datta and Nilakantan have classified all the degree-regular triangulations of closed surfaces
on at most 11 vertices.
In this article, we have proved that any degree-regular triangulation of the torus is weakly regular. We have shown that there
exists ann-vertex degree-regular triangulation of the Klein bottle if and only if n is a composite number ≥ 9. We have constructed two
distinctn-vertex weakly regular triangulations of the torus for eachn ≥ 12 and a (4m + 2)-vertex weakly regular triangulation of the Klein bottle for eachm ≥ 2. For 12 ≤n ≤ 15, we have classified all then-vertex degree-regular triangulations of the torus and the Klein bottle. There are exactly 19 such triangulations, 12 of which
are triangulations of the torus and remaining 7 are triangulations of the Klein bottle. Among the last 7, only one is weakly
regular. 相似文献
2.
This paper presents results of studies on dc electrical conductivity and transference number measurements on potassium bromate
(KBrO3) complexed polyvinyl chloride (PVC) films prepared by solution cast technique. Temperature dependence of dc electrical conductivity
and transference number data indicated the dominance of ion type charge transport in these specimens. The magnitude of conductivity
increased with increase in concentration of the salt and temperature. Using this (PVC + KBrO3) electrolyte, solid-state electrochemical cells were fabricated, and their discharge profiles were studied under a constant
load of 100 kΩ. Several cell profiles such as open circuit voltage, short circuit current, power density, and energy density
associated with these cells were evaluated and were reported. The features of complexation of the electrolytes were studied
by X-ray diffraction and Fourier transform infrared spectroscopy.
Paper presented at the Third International Conference on Ionic Devices (ICID 2006), Chennai, Tamilnadu, India, Dec. 7–9, 2006 相似文献
3.
Basudeb Datta 《Proceedings Mathematical Sciences》1994,104(2):385-388
A simplicial complex is said to satisfy complementarity if exactly one of each complementary pair of nonempty vertex-sets constitutes a face of the complex. We show that if a d-dimensional combinatorial manifold M with n vertices satisfies complementarity then d=0, 2, 4, 8, or 16 with n=3d/2+3 and |M| is a “manifold like a projective plane”. Arnoux and Marin had earlier proved the converse statement. 相似文献
4.
Let R be a prime ring of char R≠2, d a non-zero derivation of R and ρ a non-zero right ideal of R such that [[d(x),d(y)]n [y,x]m] = 0 for all x,y ∈ ρ or [[d(x),d(y)]n d[y,x]m] = 0 for all x,y ∈ ρ, n, m ≥ 0 are fixed integers. If [ρ,ρ]ρ ≠ 0, then d(ρ)ρ = 0. 相似文献
5.
Our main object in this paper is to discuss some results on rings with left identity in which certain subsets satisfy some functional identities. 相似文献
6.
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
7.
Singha K Roy A Dutta PK Tripathi S Sahabuddin S Achari B Mandal SB 《The Journal of organic chemistry》2004,69(19):6507-6510
A simple synthesis of chiral spironucleosides and spirobisnucleosides is described. Intramolecular 1,3-dipolar nitrone cycloaddition reaction of d-glucose-derived precursors having olefin at C-3 and nitrone at C-5, C-1, or C-2 (in nor-series) furnished bisisoxazolidinospirocycles 4-7, 11, and 12 in good yields. Reductive ring opening of the isoxazolidine moieties in 4-6 followed by construction of a nucleoside base upon the generated amino groups smoothly yielded spirobisnucleosides 17 and 18 and spironucleosides 20 and 21. 相似文献
8.
Mechanical and physico-chemical characterization of cyclodextrin finished polyamide fibers 总被引:2,自引:0,他引:2
Yassine El Ghoul Bernard Martel Michel Morcellet Christine Campagne Ahmida El Achari Sadok Roudesli 《Journal of inclusion phenomena and macrocyclic chemistry》2007,57(1-4):47-52
We present the study of the cyclodextrin (CDs) finishing of polyamide fibers (PA) by means of citric acid (CTR) as crosslinking agent. We observed that the mode of grafting happened by the formation of a crosslinked polymer formed between CTR and CDs. This polymer physically adhered to the fibers network and was resistant to hot water washings. Modified fibers were characterized by evaluating the contact angle with a polar liquid and by studying the hysteresis of damping of PA fibers (Cahn balance) with various grafting rates and by studying the absorptivity of grafted fabrics via the technique of the posed drop (Digidrop® instrument). Then a mechanical characterization of the PA fabrics grafted with various proportions of CDs was accomplished, by traction and tear tests by using a tensile-test bench Lohmergy. Finally a topographic study of PA grafted surfaces was approached by atomic force microscopy (AFM and LFM; contact and non-contact mode) which permitted to evaluate the roughness and the chemical heterogeneity of the grafted surfaces. 相似文献
9.
In aqueous media at 25 degrees C [Mo(CN)(8)](3-) is reduced by thioglycolic acid (HSCH(2)COOH, TGA), and the reaction is strongly accelerated by the presence of trace amounts of copper ions. Dipicolinic acid (dipic) is an effective inhibitor of the copper catalysis. Both with and without dipic the reaction has the stoichiometry 2[Mo(CN)(8)](3-) + 2TGA --> 2[Mo(CN)(8)](4-) + RSSR, where RSSR is the disulfide derived from formal oxidative dimerization of TGA. In the presence of dipic, PBN (N-tert-butyl-alpha-phenyl-nitrone), and with a large excess of TGA the rate law for consumption of [Mo(CN)(8)](3-) is first order in both [TGA] and [Mo(CN)(8)(3-)]. The complex pH dependence is consistent with (-)SCH(2)CO(2)(-) being highly reactive (k = 1.8 x 10(4) M(-1) s(-1)), the monoanion being less reactive, and HSCH(2)CO(2)H being unreactive. A mechanism is proposed in which the dianion undergoes electron transfer to [Mo(CN)(8)](3-), thus generating the thiyl radical. Analysis of the electron-transfer rate constant in terms of Marcus theory yields an effective self-exchange rate constant for the thiolate/thiyl redox couple that is in reasonable agreement with the value derived previously from the reaction of TGA with [IrCl(6)](2-). When copper catalysis is inhibited, the two reactions differ substantially in that the yield of (-)O(3)SCH(2)CO(2)(-) is significant for [IrCl(6)](2-) but undetectable for [Mo(CN)(8)](3-). 相似文献
10.
Electron transfer between [FeIII(L2)]+ and sulphur(IV) has been proposed to proceed via an inner-sphere mechanism involving formation of a transient hydrogen-bonded intermediate between the acidic proton of SO2 · xH2O/HSO3
– and the oximato oxygen of the coordinated ligand, providing the ready availability of the proton for the reduced complex. In the case of SO3
2–, this is not possible and the reaction is believed to proceed via an outer-sphere scheme. 相似文献