An Efficient Convrsion of 2′-Hydroxychalcones to Flavones

2′-Hydroxychalcones have been found to undergo smooth conversion to flavones when heated with sodium periodate in dimethyl sulphoxide.     

Development and multiplexed control of latching pneumatic valves using microfluidic logical structures

Novel latching microfluidic valve structures are developed, characterized, and controlled independently using an on-chip pneumatic demultiplexer. These structures are based on pneumatic monolithic membrane valves and depend upon their normally-closed nature. Latching valves consisting of both three- and four-valve circuits are demonstrated. Vacuum or pressure pulses as short as 120 ms are adequate to hold these latching valves open or closed for several minutes. In addition, an on-chip demultiplexer is demonstrated that requires only n pneumatic inputs to control 2(n-1) independent latching valves. These structures can reduce the size, power consumption, and cost of microfluidic analysis devices by decreasing the number of off-chip controllers. Since these valve assemblies can form the standard logic gates familiar in electronic circuit design, they should be useful in developing complex pneumatic circuits.     

Vibrational analysis of 1-chlorooctane

The organic compound 1-chlorooctane exists in liquid state at ambient temperatures and has numerous synthetic applications. Fourier transform infrared and Raman spectra of this molecule have been recorded in the range of 4000−400 cm⁻¹ and 3500−200 cm⁻¹, respectively. A detailed vibrational analysis in terms of assignment of the observed frequencies of this molecule for its four most probable conformations in liquid phase, having symmetries C _s and C _l , has been done using normal co-ordinate calculations. The force-field transferred from already studied lower chain chloro-alkanes is subjected to refinement so as to fit the observed infrared and Raman frequencies with those of calculated ones. The potential energy distribution has also been calculated for each mode of vibration of the molecule for the most probable conformations present in its liquid phase.     

Shear field modification of strongly flocculated suspensions — Aggregate morphology

Rheological and microscopical studies have been made to elucidate the effects of shear fields on the morphology of concentrated, aggregated model colloids. The models employed are well-characterised, predominantly chargestabilised polymer latices, coagulated by the addition of excess electrolyte. Continuous shear rheological and viscoelastic measurements indicate a very significant decrease in shear yield stress, apparent viscosity and shear modulus following prolonged shearing.Electron microscopy reveals the source of these changes. Freshly coagulated suspensions form networks that are porous, strong and qualitatively similar to simulated structures for diffusion limited aggregation. Following protracted shearing, the network structure is rearranged to yield discrete, tightly packed aggregates with a characteristic size, which is principally a function of the primary particle size.     

A resistless photolithography method for robust markers and electrodes

We describe a method of resistless photolithography using laser for the fabrication of microscopic markers and electrodes. A single shot of laser (355 nm, 100 mJ) is used to induce local surface melting and thus transfer a pattern from the mask (TEM grid) on to the surface of silicon. With a silicon substrate pre-coated with a layer of phosphorus, the laser pulse selectively produces doped regions that are highly conducting. The electrodes and markers thus obtained are robust and can withstand harsh chemical treatments. The utility of the marker for dip-pen nanolithography is illustrated by performing gold colloid nanopatterning.     

Engineering implementation of a hybrid optical correlator using SLMs

Optical correlators have been widely used for such applications as automatic target identification, invariant pattern recognition and machine vision. In hybrid optical correlators, Spatial light modulators (SLMs) are used to dynamically update the input and the filter. However, implementation is difficult because of the interference of “ghost” images; rigorous requirements for filter registration, accurate and effective filter sizing and complex valued filtering functions. This paper proposes some practical approaches to handle these issues and provides engineering details of how to build a hybrid optical correlator, where a SLM serves as an updateable intensity filter for real-time pattern recognition.     

Total Synthesis of (+)‐6‐epi‐Ophiobolin A

The ophiobolin sesterterpenes are notable plant pathogens which have recently elicited significant chemical and biological attention because of their intriguing carbogenic frameworks, reactive functionalities, and emerging anticancer profiles. Reported herein is a total synthesis of (+)‐6‐epi‐ophiobolin A in 14 steps, a task which addresses construction of the synthetically challenging spirocyclic tetrahydrofuran motif as well as several other key stereochemical problems. This work demonstrates a streamlined synthetic platform to complex ophiobolins leveraging disparate termination modes of a radical polycyclization cascade for divergent elaboration and functionalization.     

Complete 1H and 13C NMR assignments of six saponins from Sapindus trifoliatus

Complete 1H and 13C spectral assignments are reported for six saponins from the pericarp of Sapindus trifoliatus (Hindi name: Reetha) collected from Madhya Pradesh and Maharashtra, India, using only 1D and 2D NMR methods. The structures of the compounds were elucidated as hederagenin 3-O-(3-O-acetyl-beta-D-xylopyranosyl)-(1-3)-alpha-L-rhamnopyranosyl-(1-2)-alpha-L-ara-binopyranoside, hederagenin 3-O-(4-O-acetyl-beta-D-xylop-yranosyl)-(1-3)-alpha-L-rhamnopyranosyl-(1-2)-alpha-L-arabinop-yranoside, hederagenin 3-O-(3,4-O-diacetyl-beta-D-xylopy-ranosyl)-(1-3)-alpha-L-rhamnopyranosyl-(1-2)-alpha-L-arabinopy-ranoside, hederagenin 3-O-(3,4-O-diacetyl-alpha-L-arabinop-yranosyl)-(1-3)-alpha-L-rhamnopyranosyl-(1-2)-alpha-L-arabinop-yranoside, hederagenin 3-O-(beta-D-xylopyranosyl)-(1-3)-alpha-L-rhamnopyranosyl-(1-2)-alpha-L-arabinopyranoside and he-deragenin 3-O-(alpha-L-arabinopyranosyl)-(1-3)-alpha-L-rhamno-pyranosyl-(1-2)-alpha-L-arabinopyranoside. It is concluded that saponins of this complexity approach the limit of structural complexity, which can be solved by NMR alone, precisely and quickly.     

Stabilization of hydrated AcIII cation: the role of superatom states in actinium-water bonding

²²⁵Ac-based radiopharmaceuticals have the potential to become invaluable in designated cancer therapy. However, the limited understanding of the solution chemistry and bonding properties of actinium has hindered the development of existing and emerging targeted radiotherapeutics, which also poses a significant challenge in the discovery of new agents. Herein, we report the geometric and electronic structural properties of hydrated Ac^III cations in the [Ac^III(H₂O)_n]³⁺ (n = 4–11) complexes in aqueous solution and gas-phase using density functional theory. We found that nine water molecules coordinated to the Ac^III cation is the most stable complex due to an enhanced hydration Gibbs free energy. This complex adopts a closed-shell 18-electron configuration (1S²1P⁶1D¹⁰) of a superatom state, which indicates a non-negligible covalent character and involves H₂O → Ac^III σ donation interaction between s-/p-/d-type atomic orbitals of the Ac atom and 2p atomic orbitals of the O atoms. Furthermore, potentially existing 10-coordinated complexes need to overcome an energy barrier (>0.10 eV) caused by hydrogen bonding to convert to 9-coordination. These results imply the importance of superatom states in actinide chemistry generally, and specifically in Ac^III solution chemistry, and highlight the conversion mechanism between different coordination numbers.

The stable 9-coordinated complex adopts a closed-shell 18-electron configuration of a 1S²1P⁶1D¹⁰ jellium state, while potential 10-coordinated complexes need to overcome an energy barrier (>0.10 eV) caused by hydrogen bonding to convert to 9-coordination.     

Size dependence of the Mössbauer effect in one-dimension

Employing a model of coupled harmonic oscillators we analyze the nature of recoilless emission in the Mössbauer effect for a finite sized 1D lattice. We demonstrate explicitly that under certain assumptions, recoilless probability first attains a maximum for a certain lattice size and then decreases with increasing lattice size. Further, we derive a scaling relation for this variation. Our treatment may have relevance to the recoilless probability in finite clusters such as nanocrystals and nanowires.