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Silicone hydrogels haves been widely utilized in many in ophthalmic and other biomedical applications due to the its comfort of hydrogels, their excellent biocompatibility, high oxygen permeability and transparency. For use as a contact lens, the silicone hydrogel with interacts with the tear film, cornea, and eyelid;, thus surface properties of the gel are crucial to be considered. The highly oxygen permeabilitye performance of the silicone hydrogel contact lens materials mainly relies on the incorporationng of the siloxane functional groups., Hhowever these groups are extremely mobile and surface active, which can result in an increase in the of lens surface hydrophobicity, as well as protein and lipid deposition. Therefore, there is a need for surface modification of silicone hydrogel contact lenses. Otherwise users may might have to choose to decrease the frequency and length of wearing duration of silicone contact lenses due to dryness or bio-fouling related issues. A novel biomimetic methacrylate monomer which contains a phosphorylcholine group, 2-mMethacryloyloxyethyl pPhosphorycholine (MPC) is was grafted onto the surface of novel silicone hydrogel materials surface to create a thick hydration layer in order to enhance the protein resistance and surface wettability. Low temperature air plasma has beenwas chosen to initiate grafting polymerization of MPC monomers onto silicone hydrogel substrates. Hydrogels were treated with plasma and exposed to air flow to yield hydroperoxides on the surface; the, and peroxides group acted as a photo-initiators for further thermal MPC grafting polymerization. After surface modification, the silicone hydrogels were characterized by XPS and ATR-FTIR to confirm the structure and elemental composition. A significant amount of phosphorus element was found shown on the XPS spectra of the modified materialsum,, demonstrating that so the MPC monomers were successfully grafted onto the gel surface. According to water contact measurement results, the modified samples possessed very hydrophilic surfaces, with advancing angles of about 27°, while compared the unmodified samples at around 110°. After surface grafting, between a around 20% and to 50%’s reduction in protein deposition was also observed, which aligned with water contact angle results. Other properties such as oxygen permeability, transparency, water equilibrium, and elastic modulus remained unchanged after the air plasma exposure and thermal MPC polymerization. Thesis Master of Applied Science (MASc)

Three-Dimensional MCM (3D-MCM) is an effective method for realizing high-density assembly. In this paper, the fabrications of spacer and solder bumps, the process technology of stacked package for multi-substrates and spacer, as well as the vertical interconnection technology in research of LTCC 3D-MCM are introduced. And also the void of solder bump, the false soldering between vertical interconnection, solder choice for different soldering area in 3D-MCM are analyzed and discussed.

Treatment of potassium salts of silole dianions with donor stabilised germanium dichlorides gave the anticipated silagermafulvenylidenes R2Si = Ge(Do) (R2Si = 1-silacyclopentadiendiyl, Do = N-heterocyclic carbene (NHC)) only as transient intermediates in a side reaction. They were detected by NMR spectroscopy and, in one case, the formal dimer, 2,4-disila-1 lambda(3),3 lambda(3)-digermetane, was isolated. The main products of these reactions are sila-bis-lambda(3)-germiranes, i.e. directly interconnected digermylenes that are part of a three-membered ring. The structural data, supported by the results of density functional calculations confirm the digermylene nature of these products with a long inner cyclic Ge-Ge bond that decreases the inherent high ring strain in silagermiranes.

Nature Communications 12(1), 3383 (2021). doi:10.1038/s41467-021-23566-2, Formamidinium lead iodide perovskites are promising light-harvesting materials, yet stabilizing them under operating conditions without compromising optimal optoelectronic properties remains challenging. We report a multimodal host���guest complexation strategy to overcome this challenge using a crown ether, dibenzo-21-crown-7, which acts as a vehicle that assembles at the interface and delivers Cs+ ions into the interior while modulating the material. This provides a local gradient of doping at the nanoscale that assists in photoinduced charge separation while passivating surface and bulk defects, stabilizing the perovskite phase through a synergistic effect of the host, guest, and host���guest complex. The resulting solar cells show power conversion efficiencies exceeding 24% and enhanced operational stability, maintaining over 95% of their performance without encapsulation for 500 h under continuous operation. Moreover, the host contributes to binding lead ions, reducing their environmental impact. This supramolecular strategy illustrates the broad implications of host���guest chemistry in photovoltaics., Published by Nature Publishing Group UK, [London]

Mesoionic imidazolylidenes are recognized as excellent electron-donating ligands in organometallic and main group chemistry. However, these carbene ligands typically show poor π-accepting properties. We have performed a computational analysis of 71 mesoionic imidazolylidenes having different aryl or heteroaryl substituents in C2 position. The study has revealed that a diphenyltriazinyl (Dpt) substituent renders the corresponding carbene particularly π-acidic. The computational results could be corroborated experimentally. A mesoionic imidazolylidene with a Dpt substituent was found to be a better σ-donor and a better π-acceptor compared to an Arduengo-type N-heterocyclic carbene. To demonstrate the utility of the new carbene, we have used the ligand to stabilize a low-valent paramagnetic tin(II) compound.

Bent (hetero)allenes such as carbodicarbenes and carbodiphosphoranes can act as neutral C-donor ligands, and diverse applications in coordination chemistry have been reported. N-Heterocyclic diazoolefins are heterocumulenes, which can function in a similar fashion as L-type ligands. Herein, we describe the synthesis and the reactivity of an anionic diazoolefin. This compound displays distinct reactivity compared to neutral diazoolefins, as evidenced by the preparation of diazo compounds via protonation, alkylation, or silylation. The anionic diazoolefin can be employed as an ambidentate, X-type ligand in salt metathesis reactions with metal halide complexes. Extrusion of dinitrogen was observed in a reaction with PCl(NiPr2)2, resulting in a stable phosphinocarbene.