Cosmic acceleration in a model of scalar-tensor gravitation

In this paper we consider a model of scalar-tensor theory of gravitation in which the scalar field, $\phi$ determines the gravitational coupling G and has a Lagrangian of the form, $\mathcal{L}_{\phi} =-V(\phi)\sqrt{1 - \partial_{\mu}\phi\partial^{\mu}\phi}$. We study the cosmological consequence of this theory in the matter dominated era and show that this leads to a transition from an initial decelerated expansion to an accelerated expansion phase at the present epoch. Using observational constraints, we see that the effective equation of state today for the scalar field turns out to be $p_{\phi}=w_{\phi}{\rho}_{\phi}$, with $w_{\phi}=-0.88$ and that the transition to an accelerated phase happened at a redshift of about 0.3.Comment: 12 pages, 2 figures, matches published versio

(E)-3-Phenyl-2-(1-tosyl-1H-indol-3-ylcarbon­yl)acrylonitrile

In the title compound, C25H18N2O3S, the indole moiety is planar and makes a dihedral angle of 89.95 (09)° with the phenyl ring of the sulfonyl substituent. The mol­ecular conformation features a weak C—H⋯N short contact and the crystal packing reveals a weak C—H⋯O hydrogen bond

Self interacting Brans Dicke cosmology and Quintessence

Recent cosmological observations reveal that we are living in a flat accelerated expanding universe. In this work we have investigated the nature of the potential compatible with the power law expansion of the universe in a self interacting Brans Dicke cosmology with a perfect fluid background and have analyzed whether this potential supports the accelerated expansion. It is found that positive power law potential is relevant in this scenario and can drive accelerated expansion for negative Brans Dicke coupling parameter $\omega$. The evolution of the density perturbation is also analyzed in this scenerio and is seen that the model allows growing modes for negative $\omega$.Comment: 8pages, 5 figures, PRD style, some changes are made, figures added, reference added. To be published in Int. J. Mod. Phys.

Methyl (E)-2-[(2-nitro­phen­oxy)meth­yl]-3-phenyl­acrylate

The title compound, C17H15NO5, adopts an E conformation with respect to the C=C double bond of the phenyl­acrylate unit. The phenyl ring and methyl acrylate group of the phenyl­acrylate unit are disordered over two sets of sites with site-occupancy ratios of 0.705 (5):0.295 (5) and 0.683 (3):0.317 (3), respectively. The mean plane through the benzene ring of the phenyl acrylate makes dihedral angles of 88.4 (8) (major component) and 86.7 (8)° (minor component) with the nitro­phen­oxy ring; the dihedral angle between the two components is 3.64 (6)°. Intra­molecular C—H⋯O interactions stabilise the molecular structure. In the crystal, C—H⋯O inter­actions result in a chain of mol­ecules running along the b axis

Structural and magnetic characterization of the complete delafossite solid solution (CuAlO2){1-x}(CuCrO2){x}

We have prepared the complete delafossite solid solution series between diamagnetic CuAlO2 and the t2g^3 frustrated antiferromagnet CuCrO2. The evolution with composition x in CuAl(1-x)Cr(x)O2 of the crystal structure and magnetic properties has been studied and is reported here. The room-temperature unit cell parameters follow the Vegard law and increase with x as expected. The effective moment is equal to the Cr^3+ spin-only S = 3/2 value throughout the entire solid solution. Theta is negative, indicating that the dominant interactions are antiferromagnetic, and its magnitude increases with Cr substitution. For dilute Cr compositions, J_BB was estimated by mean-field theory to be 2.0 meV. Despite the sizable Theta, long-range antiferromagnetic order does not develop until very large x, and is preceeded by glassy behavior. Data presented here, and that on dilute Al-substitution from Okuda et al., suggest that the reduction in magnetic frustration due to the presence of non-magnetic Al does not have as dominant an effect on magnetism as chemical disorder and dilution of the magnetic exchange. For all samples, the 5 K isothermal magnetization does not saturate in fields up to 5 T and minimal hysteresis is observed. The presence of antiferromagnetic interactions is clearly evident in the sub-Brillouin behavior with a reduced magnetization per Cr atom. An inspection of the scaled Curie plot reveals that significant short-range antiferromagnetic interactions occur in CuCrO2 above its Neel temperature, consistent with its magnetic frustration. Uncompensated short-range interactions are present in the Al-substituted samples and are likely a result of chemical disorder

3-(1,2-Di-p-tolyl­vin­yl)-2-methyl-1H-indole

In the title compound, C25H23N, the indole unit makes a dihedral angles of 79.03 (5) and 61.82 (4)° with the benzene rings. No classical hydrogen bonds are found in the crystal structure

Isolation and constitution of quercetagitrin, a glucoside of quercetagetin

Quercetagitrin, a monoglucoside of quercetagetin, has for the first time been isolated from the flowers of the African Marigold (Tagetes erecta). It is not a 3-glucoside since it gives a red precipitate with lead acetate and does not undergo easy hydrolysis with acids. Further it is easily oxidised in cold alkali, and after methylation the products of decomposition yield veratric acid. The glucose group, therefore, is not present in the side phenyl nucleus. By complete methylation and subsequent hydrolysis of the glucoside, a pentamethyl quercetagetin is obtained. This ether is a new compound, and differs from 3:6:7:3':4'-pentamethyl quercetagetin in all its properties, and hence the free hydroxyl group in it is in either the 6th or the 7th position. The allyl ether of this new pentamethyl quercetagetin smoothly undergoes the Claisen Rearrangement, indicating thereby that the ortho-position with respect to the allyloxy group is unsubstituted. Hence the allyl ether should be 3:5:6:3':4'-pentamethyl-7-allyl quercetagetin, and the new pentamethyl ether should have the constitution of 3:5:6:3':4'-pentamethyl quercetagetin. Consequently quercetagitrin is the 7-glucoside of quercetagetin

Reactivity of the double bond in coumarins and related α-β unsaturated carbonyl compounds Part IV. Action of bromine on coumaric acids

By the action of bromine on coumaric, 4-methylcoumaric and 5-nitrocoumaric acids in boiling glacial acetic acid solution 3:6:8-tribromocoumarin, 3:6:8-tribromo-7-methylcoumarin and 3:8-dibromo-6-nitrocoumarin have been obtained in good yield. The primary products are the dibromides of the bromo-compounds produced by the addition at the double bond, subsequent substitution in the nucleus and final ring closure. Hydrogen bromide gets slowly removed during the boiling and during the subsequent crystallisations so as to yield the above-mentioned bromocoumarins. The best method for this however is to use cold alcoholic potash. Small quantities of the lower bromination products are also produced as by-products

Constitution of butrin

On treatment with diazomethane, butrin gives rise to a monomethyl ether which yields on hydrolysis with acids a mixture of 4'-O-methylbutin and 4'-O-methylbutein, the latter being the major component. The constitutions of these two products have been established by alkaline oxidation, yielding isovanillic acid and comparison with synthetic samples. It is, therefore, concluded that butrin is 3': 7-diglucoside of butin, and thus it is the first instance of a glycoside to contain the sugar residues in two different positions amongst the group of anthoxanthins and also the first instance to carry a sugar group in the side phenyl nucleus amongst both anthoxanthin and anthocyanin pigments

Synthetic experiments in the benzopyrone series. Part XXXIII. Synthesis of isodaidzein and its methyl ethers

This article does not have an abstract