Side‐Chain‐Functionalized Polyacetylenes, 2. Photovoltaic Properties

Polymerization of a functionalized acetylene was successfully performed using a Rh complex as the catalyst and triethylamine as a base yielding poly{(E,E,E)‐4‐[4‐[4‐(3,4,5‐tridodecyloxystyryl)‐2,5‐bis((S)‐2‐methylbutoxy)styryl]‐2,5‐bis((S)‐2‐methylbutoxy)styryl]phenylacetylene} ( PAOPV ). Films of PAOPV mixed with a fullerene derivative showed electron transfer from the OPV oligomer donor to the fullerene acceptor. The films could be furthermore used in photovoltaic devices.     

The effect of titanium dioxide exposure on the thermal properties of Zebrafish (<Emphasis Type="Italic">Danio rerio</Emphasis>) bones

This article presents the changes in the thermal properties of the control and titanium dioxide (TiO₂), both nano and bulk exposed Zebrafish bones by using thermo analytical techniques. The result shows that the mass loss due to the thermal decomposition occurs in three distinct steps due to loss of water, organic and inorganic materials. The titanium dioxide exposed bones present a different thermal behaviour compared to the control bones. The residue masses are found to be increased due to titanium dioxide exposure. In particular, nano titanium dioxide exposure increases the residue mass level significantly (three fold) when compared to titanium dioxide bulk exposure. These thermal characteristics can be used as a qualitative method to check the metal oxide intoxication in biological samples.     

Chiral (Diphosphonite)platinum Complexes in Asymmetric Hydroformylation

The chiral diphosphonite ligand (11bR,11′bR)‐4,4′‐(9,9‐dimethyl‐9H‐xanthene‐4,5‐diyl)bis[dinaphtho[2,1‐d:1′,2′‐f][1,3,2]dioxaphosphepin] ((R,R)‐XantBino; (R)‐ 1 ), based on a rigid xanthene backbone, was applied in the Pt/Sn‐catalyzed hydroformylation of styrene ( 4a ), 4‐methylstyrene ( 4b ), vinyl acetate ( 4c ), and allyl acetate ( 4d ), by using a Pt/Sn ratio of 1 : 1. High ee of up to 80% were observed, along with good regioselectivities towards the desired branched aldehydes. For styrene, an interesting inversion in the stereoselection process was observed at elevated temperatures, and a mechanism is proposed considering the temperature dependence of the regioselectivity. The complex [PtCl₂{(S,S)‐XantBino}] ((S)‐ 2 ) was characterized by X‐ray crystal‐structure analysis, revealing an unusual out‐of‐plane ligand coordination of the metal fragment. The complex [PtCl(SnCl₃){(R,R)‐XantBino}] ((R)‐ 3 ) was characterized by means of ³¹P‐NMR spectroscopy.     

Arsenic-Induced Biochemical Changes in Labeo rohita Kidney: An FTIR Study

ABSTRACT

Arsenic is a toxic heavy metal that occurs naturally in water, soil, and air. It is widespread in the environment as a consequence of both anthropogenic and natural processes. In the current study, an attempt has been made to analyze the arsenic-induced molecular changes in macromolecular components like proteins and lipids in the kidney tissues of edible fish Labeo rohita using Fourier transform infrared (FTIR) spectroscopy. The FTIR spectrum of kidney tissue is quite complex and contains several bands arising from the contribution of different functional groups. The detailed spectral analyses were performed in three distinct wave number regions, namely 3600–3050 cm^?1, 3050–2800 cm^?1, and 1800–800 cm^?1. The current study shows that the kidney tissues are more vulnerable to arsenic intoxication. FTIR spectra reveal significant differences in both absorbance intensities and areas between control and arsenic-intoxicated kidney tissues; this result indicates that arsenic intoxication induces significant alteration on the major biochemical constituents such as lipids and proteins and leads to compositional and structural changes in kidney tissues at the molecular level. The current study confirms that FTIR spectroscopy can be successfully applied to toxicologic and biological studies.