Reactivite photochimique des α-aminoenones: reactions de cyclisation et nouveau type de reaction dans les α-sulfonamido-cyclohexenones

The photochemical behaviour of 2-alkylamino 2-cyclohexenones is very sensitive to the nitrogen substituents. α-Ketoazetidines are produced by irradiation of 2-methanesulfonamido-2-cyclohexenones; however a desulfonation and aryl migration process can compete in the case of 2-arenesulfonamido-2-cyclohexenones. Furthermore divinylamine and photo-Fries rearrangements are the main reactions with 2-anilino 2-cyclohexnone and 2-benzoylamido 2-cyclohexenone respectively.     

Alkoxyallene‐ynes: Selective Preparation of Bicyclo[5.3.0] Ring Systems Including a δ‐Alkoxy Cyclopentadienone

The development of an intramolecular rhodium(I)‐catalyzed Pauson–Khand reaction of alkoxyallene‐ynes with a proximal alkoxy group is reported. This reaction, in the presence of a [Rh(cycloocta‐1,5‐diene)Cl]₂/propane‐1,3‐diylbis(diphenylphosphane) system under a CO atmosphere, constitutes a powerful tool for selectively accessing carbo‐ and heterobicyclo[5.3.0] frameworks featuring an enol ether moiety. Through this procedure, a straightforward access to guaiane skeletons with a tertiary hydroxy group at the C10 position was achieved.     

Is a polymer semiconductor having a “perfect” regular structure desirable for organic thin film transistors?

This study utilized high temperature NMR and matrix-assisted laser desorption/ionization time-of-flight (MALDI-ToF) mass spectrometry to reveal that appreciable amounts of structural defects are present in the diketopyrrolopyrrole (DPP)–quaterthiophene copolymers (PDQT) synthesized by the Stille coupling polymerization with Pd(PPh₃)₂Cl₂, Pd₂(dba)₃/P(o-tol)₃, and Pd(PPh₃)₄ catalyst systems. It was proposed that these structural defects were produced via homocoupling side reactions of the C–Br bonds and the organostannane species. Model Stille coupling reactions further substantiated that the amount of structural defects are catalyst-dependent following the order of Pd(PPh₃)₂Cl₂ > Pd₂(dba)₃/P(o-tol)₃ > Pd(PPh₃)₄. To verify the structural assignments, “perfect” structurally regular PDQT polymers were prepared using Yamamoto coupling polymerization. When compared to the structurally regular polymers, the polymers containing defects exhibited notable redshifts in their absorption spectra. Surprisingly, the “perfect” structurally regular polymers showed poor molecular ordering in thin films and very low charge transport performance as channel semiconductors in organic thin film transistors (OTFTs). On the contrary, all the “defected” polymers exhibited much improved molecular ordering and significantly higher charge carrier mobility.     

Hydroxyl chain‐end functionalization of polymeric organolithium compounds with oxetane

Hydroxyl chain‐end functionalizations of polymeric organolithium compounds with oxetane (trimethylene oxide) were studied in benzene at 25 °C. Functionalizations of poly(styryl)lithium and polystyrene‐oligo‐butadienyllithium proceed efficiently to form the corresponding ω‐hydroxypropyl‐functionalized polymers in 98 and 97% isolated yields, respectively. No nonfunctional polymer (≤1–2%) was detected by thin layer chromatography (TLC) analysis for either polymer. All functionalized polymers were characterized by ¹³C and ¹H NMR analyses; no evidence for oxetane oligomerization at the chain end was observed. The MALDI‐TOF mass spectrum of ω‐hydroxypropylpolystyrene was consistent with the expected structure without any detectable oligomerization of oxetane. A small, but detectable series of peaks corresponding to nonfunctional polystyrene was also observed in the MALDI‐TOF mass spectrum. The functionalization of the adduct of 1,1‐diphenylethylene and PSLi produced the corresponding ω‐hydroxypropyl‐functionalized polymer in only 86% isolated yield. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2684–2693, 2006     

Enhanced multiple ultrasonic shear reflection method for the determination of high frequency viscoelastic properties

In this work, we propose a study dedicated to the influence of the delay line nature in transverse ultrasonic sensors, dedicated to dynamic high frequency elastic moduli of viscoelastic materials estimation. In literature, these shear ultrasonic rheometers are using delay lines in glass or quartz and normal or oblique incidence of ultrasonic rays. The oblique incidence is used in order to improve the sensitivity of the measurements. We theoretically demonstrate in this work that the use of delay lines in polymers is recommended to improve the sensitivity. Due to modifications, performed on a 10 MHz commercial ultrasonic sensor, we experimentally show on glycerin (which is a Newtonian material) that it is possible to multiply by a factor 10 the sensitivity; compared to delay lines in quartz using a normal incidence of rays. Hence, we overpass the accuracy of the oblique incidence approach with a simpler experimental setup.     

Individual variation in the pup attraction call produced by female Australian fur seals during early lactation

Otariid seals (fur seals and sea lions) are colonial breeders with large numbers of females giving birth on land during a synchronous breeding period. Once pups are born, females alternate between feeding their young ashore and foraging at sea. Upon return, both mother and pup must relocate each other and it is thought to be primarily facilitated by vocal recognition. Vocalizations of thirteen female Australian fur seals (Arctocephalus pusillus doriferus) were recorded during the breeding seasons of December 2000 and 2001, when pups are aged from newborns to one month. The pup attraction call was examined to determine whether females produce individually distinct calls which could be used by pups as a basis for vocal recognition. Potential for individual coding, discriminant function analysis (DFA), and classification and regression tree analysis were used to determine which call features were important in separating individuals. Using the results from all three analyses: F0, MIN F and DUR were considered important in separating individuals. In 76% of cases, the PAC was classified to the correct caller, using DFA, suggesting that there is sufficient stereotypy within individual calls, and sufficient variation between them, to enable vocal recognition by pups of this species.     

Photolyse d'α-alcoxycyclanones

The photolysis of α-alkoxycyclohexanones and α-alkoxycyclopentanones in ethanol involves NII elimination of an alkoxy group. The proportion of cyclanone is higher when starting from α-alkoxycyclohexanones, and esters are isolated in low yields. No ester, but aldehydes are obtained from α-alkoxycyclopentanones. By photolysis of 2-methoxy norbornanone, only epimerisation is detected. Oxetanols are formed with satisfactory yields only from aromatic ketones such as α-methoxy tetralone or α-methoxyindanone. Mechanistic aspects, including the nature of the excited states, are discussed.