Dialkylative Cyclization Reactions of 3-(Phenylthio)-3-Sulfolenes

3-(Phenylthio)-3-sulfolene (4) underwent bridged dialkylative cyclization with 2-methylene-1,3-diiodopropane to give the bridged bicyclic 3-sulfolene 23, and spirodialkylation with 1,4-diiodobutane and 1,5-diiodopentane to give the spiro bicyclic 3-sulfolenes 15 as the major product. The reaction of 4 with 1,3-diiodopropane led to the fused bicyclic 2-sulfolene 12. 3-(Phenylthio)-3-sulfolenes bearing an ω-iodoalkyl group at the C-2 position gave the fused bicyclic 2-sulfolenes 28 and/or the spiro bicyclic 3-sulfolene 29 depending on the chain length.     

The Synthesis and Chemistry of 1,3‐Bridged Polycyclic Cyclopropenes: 8‐Oxatricyclo[3.2.1.02,4]octa‐2,6‐dienes

Three 1,3‐bridged polycyclic cyclopropenes, exo‐8‐oxatricyclo[3.2.1.0^2,4]octa‐2,6‐diene ( 10 ), endo‐8‐oxatricyclo[3.2.1.0^2,4]octa‐2,6‐diene ( 11 ), and exo‐6,7‐benzo‐1,5‐diphenyl‐8‐oxatricyclo[3.2.1.0^2,4]octa‐2,6‐diene ( 12 ), have been synthesized by elimination of 2‐chloro‐3‐trimethylsilyl‐8‐oxatricyclo[3.2.1.0^2,4]‐oct‐6‐enes, 17 , 18 and 30 , which were generated from 1‐chloro‐3‐trimethylsilylcyclopropene with furan and diphenylisobenzofuran. We have demonstrated a facile route to synthesize the highly strained 1,3‐fused polycyclic cyclopropenes, 10 , 11 , and 12 . The stereochemistry of the Diels‐Alder reactions of cyclopropene 16 with furan and DPIBF are different. Cyclopropene 16 was treated with furan to form exo‐exo and endo‐exo adducts (5:2) and treated with DPIBF to generate an exo‐exo adduct. Compounds 10 , 11 and 12 undergo isomerization reactions to form benzaldehyde and phenyl 4‐phenyl‐[1]naphthyl ketone to release strain energies via diradical mechanisms.     

Chemistry of diphenyltetrafluorophosphazene: Reactions with dilithiated diols

Reaction of gem-diphenyltetrafluorophosphazene, [1,1-(C₆H₅)₂]P₃N₃F₄ (1) with LiO(CH₂)₃OLi resulted in the formation of four products, spiro-{3,3-[O(CH₂)₃O]}[1,1-(C₆H₅)₂]P₃N₃F₂ (2), ansa-{3,5-[O(CH₂)₃O]}[1,1-(C₆H₅)₂P₃N₃F₂] (3), bridged-[1,1-(C₆H₅)₂N₃P₃F₃][O(CH₂)₃O][1,1-(C₆H₅)₂N₃P₃F₃] (4) and dangling-[HO(CH₂)₃O][1,1-(C₆H₅)₂P₃N₃F₃] (5) derivatives of 1, among which compound 5 was found to be the major product. Reaction of 1 with the dilithiated ferrocene derived diol, FcCH₂P(S)(CH₂OLi)₂ resulted in the formation of two isomers of ansa substituted fluorophosphazenes namely endo-[1,1-(C₆H₅)₂]{3,5-[FcCH₂P(S)(CH₂O)₂]}P₃N₃F₂ (6) and exo-[1,1-(C₆H₅)₂]{3,5-[FcCH₂P(S)(CH₂O)₂]}P₃N₃F₂ (7). These were formed along with the spiro isomer [1,1-(C₆H₅)₂]{3,3-[FcCH₂P(S)(CH₂O)₂]}P₃N₃F₂ (8) the dangling derivative [1,1-(C₆H₅)₂P₃N₃F₃][OCH₂(FcCH₂)P(S)CH₂OH] (9) and the bridged compound [1,1-(C₆H₅)₂P₃N₃F₃][OCH₂(FcCH₂)P(S)CH₂O][1,1-(C₆H₅)₂P₃N₃F₃] (10). All compounds were separated by column chromatography and characterized by ¹H, ³¹P{¹H}, ¹⁹F NMR, mass spectra and elemental analysis. The spirocyclic compound 8 was also characterized by X-ray crystallography.     

Synthesis of Si—H Functional Poly(phenylsilane) and Organosilane Copolymers: Low-valent Titanium Induced Polymerization of Organodichlorosilanes

在低价钛促进下,苯基二氯硅烷进行还原聚合反应生成Si-H官能化的聚苯基硅烷。应用此方法,在温和、中性反应条件下制备出Si-H官能团化的有机聚硅烷共聚物。     

The oscillatory adsorption of self‐assembled organosilane films on aluminium oxide surfaces

The time‐dependent oscillatory growth mechanism of organosilane film self‐assembly on aluminium oxide has been investigated using X‐ray photoelectron spectroscopy. While this unusual oscillatory process has been reported for the trifunctional silane, propyltrimethoxysilane, we report here, for the first time, that this oscillatory behaviour is also present during the self‐assembly of the difunctional silane propylmethyldimethoxysilane. The presence of multiple oscillations in this growth mechanism is also first reported for propyltrimethoxysilane and propylmethyldimethoxysilane as a function of exposure time. Multiple oscillations indicate that the 3‐component model that is used to describe and fit a single coverage oscillation must be reconsidered and contain additional components to account for the multiple oscillations seen experimentally. The absence of such oscillatory behaviour in the growth of the monofunctional organosilane propyldimethylmethoxysilane, which in fact follows a Langmuir‐type growth mechanism, indicates that this measurable oscillatory behaviour is because of the ability of multifunctional silanes to oligomerise both on the substrate and in solution.     

Application of the Scanning Kelvin Probe for the study of the corrosion resistance of interfacial thin organosilane films at adhesive/metal interfaces

The Scanning Kelvin Probe is introduced as a real time non-destructive in situ technique for the detection of de-adhesion at adhesive/metal oxide interfaces. Iron substrates and an epoxy adhesive served as model systems. Iron surfaces were coated with ultra-thin organosilane plasma polymer films from a microwave discharge and 3-(trimethoxysilyl)-propylamine films from dilute water based solutions. Surface and film characterisation was done by means of atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and infrared reflection absorption spectroscopy (IRRAS). The effect of these interfacial films on the stability of the adhesive/metal joint was studied in corrosive environments. The Scanning Kelvin Probe allows the measurement of electrode potentials at buried polymer/metal interfaces with a spatial resolution of about 100 m. The electrode potential characterises the reactivity of the interface. Moreover, by the variation of the oxygen partial pressure in the measurement chamber, local anodes and cathodes underneath the polymer can be distinguished. The kinetics of electrochemical de-adhesion can be effectively slowed down by thin 3-(trimethoxysilyl)-propylamine films at the interface. The effect of the adhesion promoter can be further improved when a thin SiO_x layer, which inhibits electron transfer reactions, and is deposited on the iron surface prior to coating with the adhesion promoter.This paper is dedicated to Mike Owen on occasion of his winning the DeBruyn medal, the first silicon chemist to do so.     

A Pd-mediated intramolecular ketalization of alkynediols: construction of the central [3.2.1]-bicyclic ketal core of cyclodidemniserinol trisulfate

A preliminary study dealing with the Pd-mediated alkynediol cycloisomerization to construct the central bicyclic ketal core of cyclodidemniserinol trisulfate is documented.     

Synthesis and characterization of some novel silicon esters and their application as lubricant base stock solution

A series of functional organosilanes and their esters were synthesized by the hydrosilylation reaction of Si? H group‐bearing organosilicon derivatives with maleic anhydride using Speier's catalyst and their esterification with long‐chain alcohols in the presence of stannous oxide. These products have been characterized using elemental analysis, FT‐IR, ¹H, ¹³C and ²⁹Si NMR. Viscosity, density, pour point, flash point and tribological properties of these compounds have also been evaluated. These esters have a pour point of 相似文献   

Bridged Bicyclic Lactam Enables Chemically Recyclable Nylon

Nylon, a widely-used high-performance thermoplastic, boasts exceptional durability and resistance to various solvents and weak acids, making it indispensable across diverse applications. However, its nonbiodegradable nature has led to alarming environmental pollution in land and oceans. Chemical recycling to monomers (CRM) stands as a crucial strategy for establishing a circular plastic economy, but the CRM of nylon remains largely unexplored. Herein, we introduce the bridged bicyclic lactam 5-azabicyclo[2.2.1]octan-6-one (5/6-LM), evolved from δ-valerolactam and pyrrolidone, to solve the trade-off in depolymerizability and performance. Notably, 5/6-LM exhibits nearly 95 % conversion in mild polymerization conditions and efficient depolymerization catalyzed by lewis acids. This compound is synthetically accessible from commercially available chemicals in a single step at room temperature, demonstrating high efficiency and scalability up to 50 g in laboratory. Furthermore, the resulting polyamide displays remarkable attributes including high crystallinity and thermostability up to 283 °C, significantly broadening the scope of chemically recyclable nylons.     

Synthesis of poly(ethylene glycol) (PEG)-grafted colloidal silica particles with improved stability in aqueous solvents

The known grafting procedures of colloidal silica particles with poly(ethylene glycol) (PEG) lead to grafting layers that detach from the silica surface and dissolve in water within a few days. We present a new grafting procedure of PEG onto silica with a significant improvement of the stability of the grafting layers in aqueous solvents. Moreover, the procedure avoids any dry states or other circumstances leading to strong aggregation of the particles. To achieve the improved water stability, St?ber silica particles are first pre-coated with a silane coupling agent (3-aminopropyl)triethoxysilane (APS) to incorporate active amine groups. The water solubility of the pre-coating layer was minimized using a combination of APS with bis-(trimethoxysilylpropyl)amine (BTMOSPA) or bis-(triethoxysilyl)ethane (BTEOSE). These pre-coated particles were then reacted with N-succinimidyl ester of mono-methoxy poly(ethylene glycol) carboxylic acid to form PEG-grafted silica particles. The particles form stable dispersions in aqueous solutions as well as several organic solvents.