A join graph denoted by G + H,is illustrated by connecting each vertex of graph G to each vertex of graph H.In this paper,we prove the crossing number of join product of K_5 + P_n is Z(5,n) + 2 n + [n/2] + 4 for n ≥ 2. 相似文献
In this paper, we give the definition of weak WT2-class of differential forms, and then obtain its weak reverse Holder inequality. As an application, we give an alternative proof of the higher integrability result of weakly A-harmonic tensors due to B. Stroffolini. 相似文献
Let L =△ + V be a SchrSdinger operator in Rd, d ≥ 3, where the nonnegative potential V belongs to the reverse HSlder class Sd. We establish the BMOL-boundedness of Riesz transforms З/ЗxiL-1/2, and give the Fefferman-Stein type decomposition of BMOL functions. 相似文献
In this paper we consider the SchrSdinger operator -△G + W on the nilpotent Lie group G where the nonnegative potential W belongs to the reverse H51der class Bq1 for some q1 ≥ D and D is the dimension at infinity of G. The weighted L^p -L6q estimates for the operators W^a(-△G + W)^-β and W^a△G(-△G + W)^-β are obtained. 相似文献
An iron‐mediated reverse ATRP of methyl methacrylate (MMA) is successfully carried out in water in the absence of any dispersants, using a water‐soluble 2,2′‐azobis(2‐methylpropionamidine) dihydrochloride (V‐50) as the initiator and the stabilizer, and using an oil‐soluble N,N‐butyldithiocarbamate ferrum (Fe(S2CN(C4H9)2)3) as the catalyst without adding any additional ligands. Micron‐sized PMMA particles with UV light‐sensitive ‐S2CN(C4H9)2 end group are obtained, and monomer droplet nucleation and suspension polymerization mechanism are proposed. Polymerization results demonstrated typical “living”/controlled characteristics of ATRP: first‐order polymerization kinetics, linear increase of molecular weights with monomer conversion and narrow molecular weight distributions for the resultant PMMA particles. NMR spectroscopy and chain‐extension experiments under UV light irradiation confirm the attachment and livingness of UV light‐sensitive ‐S2CN(C4H9)2 group in the chain end.
Formation of reverse micelles in the water–hexane–AOT system has been investigated by molecular dynamics simulations. In order to optimize calculation strategy, the starting spatial disposition of components was assumed to be random. Such an approach was found to provide a lower dependence of final results on initial conditions as compared to the calculations using pre-assembled reverse micelles as a starting geometry. The calculated structural parameters of reverse micelles (such as their shape, size, and distribution of components) were found to agree with the available experimental data. 相似文献