2,8,10,11-tetrachloro-12-oxahexacyclo-[7.2.1.02,8.03,7.04,11.06,10]dodeca-1,9-diol and disorder and mixed crystals in a system of tetracyclo-[6.3.0.04,11.05,9]undecanone and undecanol derivatives

2,8,10,11-Tetrachloro-12-oxahexacyclo[7,2.1.0^2.8.0^3.7.0^4.11.0^6.10]dodeca-1,9-diol is a strained cage molecule containing six five-membered rings and a four-membered ring. Twenty-five of the internal angles are less than 105° with 6 ranging from 89.5(3) to 97.4(3)°. The base promoted reaction of 3,6-dipyridyl-1,2,4,5-tetrazine with tetracyclo[6.3.0.0^4.11.0^5.9]undecane-3,6-dione yields the monoketone 6,7-[3,6-di(2-pyridyl)-4,5-pyridizino]tetracyclo[6.3.0.0^4.11.0^5.9]-undecan-2-one. This compound crystallizes in the centrosymmetric space group P2₁/n with enantiomers related by a center of symmetry. In the crystal investigated the molecules are disordered with each site containing about 80% of one isomer and 20% of the enantiomer. When the ketone is hydrogenated and the product isolated, two different crystals were found to have a ratio of alcohol to ketone of .71/.29 and .75/.25 or about 3/1. The alcohol and ketone occupy the same sites, but with opposite stereochemistries.     

On the service system MX/G/∞

In the present paper we consider the service system M^X/G/∞ characterized by an infinite number of servers anda general service time distribution. The customers arrive at the system in groups of size X, which is a random variable, the time between group arrivals being exponentially distributed. Using simple probability arguments, we obtain probability generating functions (p.g.f.'s) of the number of busy servers at time t and the number that depart by time t. Several other properties of these random variables are also discussed.     

Experimental and Theoretical Study of High Temperature-Stability and Low-Chirp 1.55 µm Semiconductor Laser with an External Fiber Grating

An experimental and theoretical study of the effect of temperature on the static and dynamic characteristics of packaged external fiber grating semiconductor lasers (FGL) is reported on. Operating in single frequency mode, the laser exhibits high output power (> 8 mW), high temperature stability of operating frequency (-3.4 GHz/K), and low static chirp (-60 MHz/mA). The observed hysteresis in wavelength versus temperature dependence is explained in the frame of a time-domain FGL model accounting for asymmetric nonlinear gain. The laser has low dynamic chirp (~16 MHz/mA) under 2.5 GB/s direct modulation, which is the key factor determining low penalty transmission over 312 km of SSM fiber. Dense WDM transmission performed at 2.6 Gbit/s over 117 km of SSM fiber shows that an FGL-based transmitter is a factor of 7 more tolerant to temperature variations than externally modulated DFB lasers.     

Synchrotron X‐ray phase contrast imaging of leaf venation in soybean (Glycine max) after exclusion of solar UV (280–400 nm) radiation

The hydraulic efficiency of a leaf depends on its vascular structure as this is responsible for transport activities. To investigate the effect of exclusion of UVAB and UVB radiation from the solar spectrum on the micro‐structure of leaves of soybean (Glycine max, variety JS‐335), a field experiment was conducted using synchrotron‐based phase contrast imaging (PCI). Plants were grown in specially designed UV exclusion chambers, and wrapped with filters that excluded UVB (280–315 nm) or UVAB (280–400 nm), or transmitted all the ambient solar UV (280–400 nm) radiation (filter control). Qualitative observation of high‐resolution X‐ray PCI images obtained at 10 keV has shown the differences in major and minor vein structures of the leaves. The mid‐rib width of the middle leaflet of third trifoliate leaves, for all treatments, were obtained using quantitative image analysis. The width of the mid‐rib of the middle leaflet of third trifoliate leaves of UVB excluded plants was found to be more compared to leaves of filter control plants, which are exposed to ambient UV. The mid‐rib or the main conducting vein transports water and sugars to the whole plant; therefore, mid‐rib enhancement by the exclusion of solar UV radiation possibly implies enhancement in the leaf area which in turn causes an increased rate of photosynthesis.     

Supramolecular Control of Singlet Oxygen Generation

Singlet oxygen (¹O₂) is the excited state electronic isomer and a reactive form of molecular oxygen, which is most efficiently produced through the photosensitized excitation of ambient triplet oxygen. Photochemical singlet oxygen generation (SOG) has received tremendous attention historically, both for its practical application as well as for the fundamental aspects of its reactivity. Applications of singlet oxygen in medicine, wastewater treatment, microbial disinfection, and synthetic chemistry are the direct results of active past research into this reaction. Such advancements were achieved through design factors focused predominantly on the photosensitizer (PS), whose photoactivity is relegated to self-regulated structure and energetics in ground and excited states. However, the relatively new supramolecular approach of dictating molecular structure through non-bonding interactions has allowed photochemists to render otherwise inactive or less effective PSs as efficient ¹O₂ generators. This concise and first of its kind review aims to compile progress in SOG research achieved through supramolecular photochemistry in an effort to serve as a reference for future research in this direction. The aim of this review is to highlight the value in the supramolecular photochemistry approach to tapping the unexploited technological potential within this historic reaction.     

Temperature-dependent structure of methyltributylammonium bis(trifluoromethylsulfonyl)amide: X ray scattering and simulations

We report the combined results of computational and x ray scattering studies of amorphous methyltributylammonium bis(trifluoromethylsulfonyl)amide as a function of temperature. These studies included the temperature range for the normal isotropic liquid, a deeply supercooled liquid and the glass. The low q peaks in the range from 0.3 to 1.5 A(-1) in the structure function of this liquid can be properly accounted for by correlations between first and second nearest neighbors. The lowest q peak can be assigned to real space correlations between ions of the same charge, while the second peak arises mostly from nearest neighbors of opposite charge. Peaks at larger q values are mostly intramolecular in nature. While our simulated structure functions provide an excellent match to our experimental results and our experimental findings agree with previous studies reported for this liquid, the prior interpretation of the experimental data in terms of an interdigitated smectic A phase is not supported by our simulations. In this work, we introduce a set of general theoretical partitions of real and reciprocal space correlations that allow for unambiguous analysis of all intra- and interionic contributions to the structure function and coherent scattering intensity. We find that the intermolecular contributions to the x ray scattering intensity are dominated by the anions and cross terms between cations and anions for this ionic liquid.     

Photo-physical aspects of BODIPY-coumarin conjugated sensor and detection of Al3+ in MCF-7 cell

ABSTRACT

BODIPY azine bearing chemosensor R1 has been synthesised for selective detection of Al³⁺with visual colour change from red-purple to purple and photo-physical studies were explained through Förster Resonance Energy Transfer (FRET) mechanism. Chemosensor showed good sensing capability with high binding constant and lower Limit of Detection (LOD) towards Al³⁺. Cell viability and fluorescence microscopic experiments illustrated about the cytocompatibily of the sensor in presence of Al³⁺ in living cells (MCF-7).     

Synthesis of hexacyclo[7.4.0.02,8.03,7.06,11]Tridecane-10,13-dione(“homosecohexaprismane-10,13-dione”)

HEXACYCLO[7.4.0.0^2,8.0^3,7.0^6,11]tridecane-10,13-dione (“homosecohexaprismane-10,13-dione”, 8) has been prepared via a six-step sequence that results in homologation of two of the cyclopentane rings in pentacyclo[5.4.0.0^2,6.0^3,10.0^5,9]-undecane-8,11-dione, 1. The structure of 8 has been established unequivocally via single crystal X-ray structural analysis.