Chitosan nanoreactor modified with PNIPAAm as efficient catalyst for preparation of chiral boron compounds in aqueous phase.

This work constructed chitosan-based core-shell catalytic nanoreactor (CS/NI/SA@Cu(II)) by free radical polymerization of biomass chitosan and temperature sensitive materials. The CS/NI/SA@Cu(II) were characterized by FT-IR, TG, XPS, SEM, TEM, and EDS to prove the formation of the nanoreactor, and the Cu content was obtained by ICP analysis. The TEM indicated that CS/NI/SA-2 presented a hollow core-shell structure with a size of about 100 nm, and the contact angle of CS/NI/SA-2 was 67°.

Total net-rate of 27.88 Tb/s full C-band transmission over 4,550 km using 150 km span length and high-gain EDFA amplification.

We experimentally demonstrate a total net-rate of 27.88 Tb/s for C-band wavelength-division multiplexing (WDM) transmission over an ultralong span-length of 150 km. It is the largest net capacity × span-length product of 4182 Tb/s·km for C-band, single-core, standard single-mode optical fiber transmission over a length of more than 3,000 km.

Cellulose supported TiO/CuO for highly asymmetric conjugate addition of α,β-unsaturated compounds in aqueous phase.

A series of new kind green cellulose-supported bimetallic TiO/CuO (Cell@TiO/CuO) catalytic materials were obtained by in-situ reduction method employing cellulose as the carrier. The effects of metal percentage composition on the morphology and construction of the catalytic materials were systematically investigated. The Cell@TiO/CuO were characterized by FT-IR, TG, XPS, SEM, TEM, EDS, and the element content was obtained by elemental analysis.

Application of Chitosan/Poly(vinyl alcohol) Stabilized Copper Film Materials for the Borylation of α, β-Unsaturated Ketones, Morita-Baylis-Hillman Alcohols and Esters in Aqueous Phase.

A chitosan/poly(vinyl alcohol)-stabilized copper nanoparticle (CP@Cu NPs) was used as a heterogeneous catalyst for the borylation of α, β-unsaturated ketones, MBH alcohols, and MBH esters in mild conditions. This catalyst not only demonstrated remarkable efficiency in synthesizing organoboron compounds but also still maintained excellent reactivity and stability even after seven recycled uses of the catalyst. This methodology provides a gentle and efficient approach to synthesize the organoboron compounds by efficiently constructing carbon-boron bonds.