A facile Garratt–Braverman cyclization route to intercalative DNA-binding bis-quinones

Bispropargyl ethers (both symmetrical and non-symmetrical) equipped with 1,4-dimethoxyaryl groups were synthesized. Under strongly basic conditions (KOBu^t/toluene/reflux), these ethers underwent Garratt–Braverman type cyclization to the tetramethoxy bi-aryl systems in high yields presumably via the bisallenes. The products could be successfully converted to the bis-quinones via CAN-mediated demethylation cum oxidation. This two-step protocol offers a simple route to bis-quinones, connected by C1–C2′ bonds, in good yields. Fluorescence based EB-displacement assay, CD spectroscopy and viscosity measurements confirmed the DNA-binding ability of the synthesized quinones via intercalation.     

Telechelic Poly(disulfide)s and Related Block Copolymer

In this communication, a mild, efficient, and generalized polycondensation route is developed for poly(disulfide)s from commercially available monomers 2,2′‐dithiodipyridine and 1,6‐hexanedithiol. Using the stoichiometric imbalance between the two monomers, it is possible to produce telechelic poly(disulfide)s of predictable molecular weight with reactive pyridyl disulfide groups at both the terminals of the chain. The two terminal pyridyl disulfide groups can be quantitatively replaced by a functional thiol using selective thiol‐disulfide exchange and thus produces functional telechelic poly(disulfide)s, which can be used as a macroinitiator to initiate ring‐opening poly­merization of a cyclic lactide monomer generating an ABA‐type triblock copolymer with degradable B block.

     

QSPR checking and validation: a case study with hydroxy radical reaction rate constant

Traditionally, QSAR and QSPR models have been fitted by splitting the available compounds into separate learning and validation sets. The model is then fitted to the learning set and assessed using the validation set. Cross-validation (CV) uses all available compounds for both purposes, so that the full body of available information is brought to bear on both the learning and the validation portions of the study. The price paid for this additional information is a substantially greater computational load. A common mistake in using CV is to omit some of the repetitive computations. This mistake leads to substantial bias in the assessment. A hydroxyl radical reaction rate dataset is used to illustrate the superiority of CV and the pitfalls from its improper execution when modeling using nearest neighbors, paralleling behavior in the well-studied linear model setting.     

Thermo‐mechanical Properties of PEO‐PU/PAN Semi‐Interpenetrating Polymer Networks and their LiClO4 Salt‐Complexes

This paper is an investigation on the thermo‐mechanical properties of a new class of materials, which holds promise for its potential use as solid polymer electrolytes, i.e., SPE material. A series of poly(ethylene oxide)‐polyurethane/poly(acrylonitrile) (PEO‐PU/PAN) semi‐IPNs, along with their LiClO₄ salt complexes, were characterized for their thermal, mechanical and dimensional stability using DSC, TG‐DTA, UTM and DMTA. The glass transition temperature (T_g) of both the undoped and doped semi‐IPNs, obtained by DSC, remained well below room temperature (～?50°C to ?35°C), satisfying one of the essential requirements to serve as a SPE host matrix. The crystallization process in the PEO segments of the PEO‐PU/PAN semi‐IPNs was prevented at higher salt concentrations, which is attributed to the Li⁺ ion mediated pseudo‐crosslinks. Good thermal stability of the semi‐IPNs was evident from the degradation onset temperature (T₀～240°C) with a three‐stage degradation process, which is independent of the PAN content as observed from differential thermogravimetric studies. The incorporation of PAN in the PEO‐PU networks results in improved mechanical properties, such as tensile strength and modulus while retaining the flexibility of the semi‐IPNs. The peak temperatures and storage modulus obtained from DMTA correlates well with the observations of DSC and tensile measurements.     

A simple and sensitive separation technique of 99Mo and 99mTc from their equilibrium mixture

The present work describes a simple and inexpensive separation method of ⁹⁹Mo from the equilibrium mixture. The liquid–liquid extraction technique has been employed to separate ⁹⁹Mo and ^99mTc using triisooctylamine (TIOA). The ⁹⁹Mo and ^99mTc were quantitatively separated out in 2 M TIOA with tripled distilled water; ^99mTc was back extracted from TIOA organic phase to aqueous phase by 0.1 M DTPA. The species information or indirect speciation of molybdenum was also established by the extraction profile of the molybdenum.     

Alteration in metal ion induced fluorescence signaling responses of benzofurazan appended acyclic amino-receptor through its structural modification

Fluorescent signaling probes 3 and 4 in the integrated ‘fluorophore-receptor’ format have been synthesized by derivatization of ‘amino-alkyl-amino’ based receptors with 7-chloro-4-nitrobenz-2-oxa-1,3-diazole fluorophore for metal ion induced fluorescence recovery through perturbation of charge-transfer character of fluorophoric D(donor)−π−A(acceptor) segment. Among all the metal ions investigated, the ‘amino-ethyl-amino’ receptor based probe 3 exhibits fluorescence enhancement selectively in presence of Zn(II) ion, while the probe 4 with an structurally modified ‘amino-ethyl-oxy-(phenyl methyl)-amino’ based receptor exhibits fluorescence enhancement with Co(II), Ni(II), Cu(II), Zn(II), and Ag(I). The chemo-selectivity of 3 towards Zn(II) ion fails in 4 due to a structural modification to receptor's framework.