Muhammad Amirul Islam

Borane-catalyzed room-temperature hydrosilylation of alkenes/alkynes on silicon nanocrystal surfaces.

Room-temperature borane-catalyzed functionalization of hydride-terminated silicon nanocrystals (H-SiNCs) with alkenes/alkynes is reported. This new methodology affords formation of alkyl and alkynyl surface monolayers of varied chain lengths (i.e., C5-C12). The present study also indicates alkynes react more readily with H-SiNC surfaces than equivalent alkenes. Unlike other toxic transition-metal catalysts, borane or related byproducts can be readily removed from the functionalized SiNCs. The new method affords stable luminescent alkyl/alkenyl-functionalized SiNCs.

Alkoxy-Terminated Si Surfaces: A New Reactive Platform for the Functionalization and Derivatization of Silicon Quantum Dots

Alkoxy-terminated silicon quantum dots (SiQDs) were synthesized via hydrosilylation of aliphatic ketones on hydride-terminated SiQD (H-SiQD) surfaces under microwave-irradiation. Aromatic ketones undergo hydrosilylation on H-SiQD surfaces at room temperature without requiring any catalyst. The alkoxy-terminated SiQDs are soluble in organic solvents, colloidally stable, and show bright and size dependent photoluminescence (PL). The alkoxy-functionalized silicon surfaces were used as reactive platform for further functionalization via unprecedented ligand exchange of the alkoxy-surface groups with alkyl or alkenyl-surface groups in the presence of BH3·THF. Proton nuclear magnetic resonance ((1)H NMR), Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS) spectroscopy confirmed alkoxy-terminated surfaces and their ligand exchange reactions in the presence of various alkenes and alkynes.

Chloride surface terminated silicon nanocrystal mediated synthesis of poly(3-hexylthiophene).

Abundant and environmentally benign metal-free silicon-based reagents, including chloride surface-terminated silicon nanocrystals (Cl-SiNCs) and silicon wafers as well as molecular chlorosilanes, were explored as catalysts for the synthesis of poly-3-hexylthiophene (P3HT) at room temperature. Cl-SiNC catalysts exhibit the highest activity of those investigated, and systems based upon single-crystal silicon wafers provide convenient, straightforward purification. The as-prepared P3HT exhibits moderate molecular weights and bears H/Br or Br/Br end groups; these properties will allow direct application and also facilitate their use as macroinitiators in the syntheses of block and/or telechelic polymers. The silicon-based systems are expected to provide an efficient metal-free catalytic preparation of functional polymers.

Phosphorus Pentachloride Initiated Functionalization of Silicon Nanocrystals

Phosphorus pentachloride (PCl5) has long been used to chlorinate hydrocarbons. It has also been applied in silicon surface chemistry to facilitate alkylation via a two-step halogenation/Grignard route. Here we report a study of the reaction of PCl5 with hydride-terminated silicon nanocrystals (H-SiNCs). An examination of the reaction mechanism has allowed us to establish a functionalization protocol that uses PCl5 as a surface radical initiator to introduce alkyl and alkenyl moieties to the surface of H-SiNCs. The reaction proceeds quickly in a single step, at room temperature and the functionalized silicon nanocrystals retained their morphology and crystallinity. The resulting materials exhibited size-dependent photoluminescence that was approximately 3× as bright as that observed for thermally hydrosilylated SiNCs. Furthermore, the absolute PL quantum yield (AQY) was more than double. The high AQY is expected to enable SiNCs to compete with chalcogenide-based quantum dots in various applications.

Influence of electrode assembly on catalytic activation and deactivation of a Pt film immobilized H + conducting solid electrolyte in electrocatalytic reduction reactions

Symmetric (Cu–Pt|Nafion|Pt–Cu) and asymmetric (Pt|Nafion|Pt–Cu) assemblies were fabricated to study the nitrate reduction processes at the cathode. The electrocatalytic nitrate reduction reactions were performed in these assemblies in order to investigate the prerequisite for the enhanced catalytic activity, electrochemical cell durability as well as preferable product selectivity resulting from the reduction of nitrate at the cathode. It has been observed for the symmetric assembly that Cu particles were oxidized on the anode surface under an applied potential and the resulting copper ions migrated to the cathode surface through the Nafion membrane, which deposited as copper oxide on the cathode surface. The formation of this copper oxide covering layer on the Pt–Cu cathode surface is attributed as the reason for the deactivation of the cathode that governed the reduced nitrate reduction along with increasing nitrite selectivity. These problems were addressed and resolved with the asymmetric design of the electrocatalytic reactor, where enhanced hydrogen evolution activates the surface by eroding the CuO over layer as well as speeding up the slow rate determining hydrogenation reactions.

Grafting Poly(3-hexylthiophene) from Silicon Nanocrystal Surfaces: Synthesis and Properties of a Functional Hybrid Material with Direct Interfacial Contact

Hybrid functional materials (HFMs) comprised of semiconductor nanoparticles and conjugated polymers offer the potential of synergetic photophysical properties. We have developed HFMs based upon silicon nanocrystals (SiNCs) and the conductive polymer poly(3-hexylthiophene) (SiNC@P3HT) by applying surface-initiated Kumada catalyst transfer polycondensation (SI-KCTP). One unique characteristic of the developed SiNC@P3HT is the formation of a direct covalent bonding between SiNCs and P3HT. The presented method for obtaining direct interfacial attachment, which is not accessible using other methods, may allow for the development of materials with efficient electronic communication at the donor-acceptor interfaces. Systematic characterization provides evidence of a core-shell structure, enhanced interfacial electron and/or energy transfer between the P3HT and SiNC components, as well as formation of a type-II heterostructure.

Instantaneous Functionalization of Chemically Etched Silicon Nanocrystal Surfaces

Remarkable advances in surface hydrosilylation reactions of C=C and C=O bonds on hydride-terminated silicon have revolutionized silicon surface functionalization. However, existing methods for functionalizing hydride-terminated Si nanocrystals (H-SiNCs) require long reaction times and elevated temperatures. Herein, we report a room-temperature method for functionalizing H-SiNC surfaces within seconds by stripping outermost atoms on H-SiNC surfaces with xenon difluoride (XeF2 ). Detailed analysis of the reaction byproducts by in situ NMR spectroscopy and GC-MS provided unprecedented insight into NC surface composition and reactivity as well as the complex reaction mechanism of XeF2 activated hydrosilylation.

Functional Bioinorganic Hybrids from Enzymes and Luminescent Silicon-Based Nanoparticles

This study reports the preparation of functional bioinorganic hybrid materials exhibiting catalytic activity and photoluminescent properties arising from the combination of enzymes and freestanding silicon-based nanoparticles. The hybrid materials reported herein have potential applications in biological sensing/imaging and theranostics, as they combine long-lived silicon-based nanoparticle photoluminescence with substrate-specific enzymatic activity. Thermal hydrosilylation of undecenoic acid and alkene-terminated poly(ethylene oxide) with hydride-terminated silicon nanocrystals afforded nanoparticles functionalized with a mixed surface made up of carboxylic acid and poly(ethylene oxide) moieties. These silicon-based nanoparticles were subsequently conjugated with prototypical enzymes through the carbodiimide-mediated amide coupling reaction in order to form bioinorganic hybrids that display solubility and photostability in phosphate buffer, photoluminescence (λmax = 630 nm), and enzymatic activity. They were characterized using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), dynamic light scattering analysis (DLS), photoluminescence spectroscopy, and pertinent enzyme activity assays.

A review on genotoxic and mutagenic effects of monoterpenes

This review sketches genotoxic and mutagenic potentials of monoterpenes, which find outs some important genotoxic, mutagenic as well as non-genotoxic and non-mutagenic monoterpenes. Monoterpenes are the important natural products.

Genetics and current treatment strategy of colorectal cancer

This review aims to sketch a current scenario of colorectal cancer (CRC). Findings say that males are the most susceptible to CRC than the females. BRAF and RAS mutations are known as common causes of CRC. Not only targeted therapy but also a combination of radio- and chemotherapy is very useful in CRC.