Saradaferin, a new sesquiterpenoid coumarin from Ferula assafoetida

Phytochemical investigation of the gum resin of Ferula assafoetida resulted in the isolation and characterization of a new sesquiterpenoid coumarin, Saradaferin (1) named as [Decahydro-(3-alpha-hydroxy-4,4,10-trimethyl-8-methylene-9-naphthenyl)-alpha-hydroxymethyl] ether of umbelliferone.     

How happy is your web browsing? A model to quantify satisfaction of an Internet user searching for desired information

We feel happy when web browsing operations provide us with necessary information; otherwise, we feel bitter. How to measure this happiness (or bitterness)? How does the profile of happiness grow and decay during the course of web browsing? We propose a probabilistic framework that models the evolution of user satisfaction, on top of his/her continuous frustration at not finding the required information. It is found that the cumulative satisfaction profile of a web-searching individual can be modeled effectively as the sum of a random number of random terms, where each term is a mutually independent random variable, originating from ‘memoryless’ Poisson flow. Evolution of satisfaction over the entire time interval of a user’s browsing was modeled using auto-correlation analysis. A utilitarian marker, a magnitude of greater than unity of which describes happy web-searching operations, and an empirical limit that connects user’s satisfaction with his frustration level—are proposed too. The presence of pertinent information in the very first page of a website and magnitude of the decay parameter of user satisfaction (frustration, irritation etc.) are found to be two key aspects that dominate the web user’s psychology. The proposed model employed different combinations of decay parameter, searching time and number of helpful websites. The obtained results are found to match the results from three real-life case studies.     

Minimal polar swimmer at low Reynolds number

We propose a minimal model for a polar swimmer, consisting of two spheres connected by a rigid slender arm, at low Reynolds number. The propulsive velocity for the proposed model is the maximum for any swimming cycle with the same variations in its two degrees of freedom and its displacement in a cycle is achieved entirely in one step. The stroke averaged flow field generated by the contractile swimmer at large distances is found to be dipolar. In addition, the changing radius of one of the spheres generates the field of a potential doublet centered at its initial position.     

N-Heterocyclic Olefins on a Silicon Surface

The adsorption of N-heterocyclic olefins (NHOs) on silicon is investigated in a combined scanning tunneling microscopy, X-ray photoelectron spectroscopy, and density functional theory study. We find that both of the studied NHOs bind covalently, with ylidic character, to the silicon adatoms of the substrate and exhibit good thermal stability. The adsorption geometry strongly depends on the N-substituents: for large N-substituents, an upright adsorption geometry is favored, while a flat-lying geometry is found for the NHO with smaller wingtips. These different geometries strongly influence the quality and properties of the obtained monolayers. The upright geometry leads to the formation of ordered monolayers, whereas the flat-lying NHOs yield a mostly disordered, but denser, monolayer. The obtained monolayers both show large work function reductions, as the higher density of the flat-lying monolayer is found to compensate for the smaller vertical dipole moments. Our findings offer new prospects in the design of tailor-made ligand structures in organic electronics and optoelectronics, catalysis, and material science.     

Pd-Catalyzed Regioselective Domino C−C Bond Formation to Access N-Fused Benzimidazo-Indolo-Isoquinoline Heterocycles

Regioselective synthesis of N-fused benzimidazo-indolo-isoquinoline heterocycles via Pd-catalyzed domino coupling reaction of 1-(1-methyl-1H-indol-2-yl)-1H-benzimidazoles and aryl halides was developed. This one pot methodology proceeded via a five-member carbopalladacycle intermediate and provided direct and facile route to access structurally complex polyheterocycles in moderate to good yields. These unique hybrid molecules resembled structural similarity with naturally isolated alkaloids. Notably, the present domino process occurred through activation of three C−H bonds and the simultaneous formation of two new C−C bonds in one-shot. These molecules exhibited strong solid and solution phase fluorescence and their emission spectra in both the medium are reported here.