Nanomaterials are engineered structures with at least one dimension of 100 nanometers or less. These materials are increasingly being used for commercial purposes such as fillers, opacifiers, catalysts, semiconductors, cosmetics, microelectronics, and drug carriers. Materials in this size range may approach the length scale at which some specific physical or chemical interactions with their environment can occur. As a result, their properties differ substantially from those bulk materials of the same composition, allowing them to perform exceptional feats of conductivity, reactivity, and optical sensitivity. Possible undesirable results of these capabilities are harmful interactions with biological systems and the environment, with the potential to generate toxicity. The establishment of principles and test procedures to ensure safe manufacture and use of nanomaterials in the marketplace is urgently required and achievable.

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Toxic Potential of Materials at the Nanolevel

-phenylenevinylene)s L4. Fluorene-Based Conjugated Polymers L4.1. Fluorene-Based Copolymers ContainingElectron-Rich MoietiesM4.2. Fluorene-Based Copolymers ContainingElectron-Deﬁcient MoietiesN4.3. Fluorene-Based Copolymers ContainingPhosphorescent ComplexesQ5. Carbazole-Based Conjugated Polymers R5.1. Poly(2,7-carbazole)-Based Polymers R5.2. Indolo[3,2-

https://ir.nctu.edu.tw:443/bitstream/11536/6508/1/000271856900020.pdf

Synthesis of Conjugated Polymers for Organic Solar Cell Applications

Pick your Pd partners: A number of catalytic systems have been developed for palladium-catalyzed CH activation/CC bond formation. Recent studies concerning the palladium(II)-catalyzed coupling of CH bonds with organometallic reagents through a PdII/Pd0 catalytic cycle are discussed (see scheme), and the versatility and practicality of this new mode of catalysis are presented. Unaddressed questions and the potential for development in the field are also addressed.

In the past decade, palladium-catalyzed CH activation/CC bond-forming reactions have emerged as promising new catalytic transformations; however, development in this field is still at an early stage compared to the state of the art in cross-coupling reactions using aryl and alkyl halides. This Review begins with a brief introduction of four extensively investigated modes of catalysis for forming CC bonds from CH bonds: PdII/Pd0, PdII/PdIV, Pd0/PdII/PdIV, and Pd0/PdII catalysis. A more detailed discussion is then directed towards the recent development of palladium(II)-catalyzed coupling of CH bonds with organometallic reagents through a PdII/Pd0 catalytic cycle. Despite the progress made to date, improving the versatility and practicality of this new reaction remains a tremendous challenge.

/pdf/palladium-ii-catalyzed-c-h-activation-c-c-cross-coupling-2546yox1wp.pdf

Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.

Over the past few decades, researchers have established artificial enzymes as highly stable and low-cost alternatives to natural enzymes in a wide range of applications. A variety of materials including cyclodextrins, metal complexes, porphyrins, polymers, dendrimers and biomolecules have been extensively explored to mimic the structures and functions of naturally occurring enzymes. Recently, some nanomaterials have been found to exhibit unexpected enzyme-like activities, and great advances have been made in this area due to the tremendous progress in nano-research and the unique characteristics of nanomaterials. To highlight the progress in the field of nanomaterial-based artificial enzymes (nanozymes), this review discusses various nanomaterials that have been explored to mimic different kinds of enzymes. We cover their kinetics, mechanisms and applications in numerous fields, from biosensing and immunoassays, to stem cell growth and pollutant removal. We also summarize several approaches to tune the activities of nanozymes. Finally, we make comparisons between nanozymes and other catalytic materials (other artificial enzymes, natural enzymes, organic catalysts and nanomaterial-based catalysts) and address the current challenges and future directions (302 references).

Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes

The recent advances in nanotechnology and the corresponding increase in the use of nanomaterials in products in every sector of society have resulted in uncertainties regarding environmental impacts. The objectives of this review are to introduce the key aspects pertaining to nanomaterials in the environment and to discuss what is known concerning their fate, behavior, disposition, and toxicity, with a particular focus on those that make up manufactured nanomaterials. This review critiques existing nanomaterial research in freshwater, marine, and soil environments. It illustrates the paucity of existing research and demonstrates the need for additional research. Environmental scientists are encouraged to base this research on existing studies on colloidal behavior and toxicology. The need for standard reference and testing materials as well as methodology for suspension preparation and testing is also discussed.

Nanomaterials in the environment: Behavior, fate, bioavailability, and effects

Two regioisomers with C3 or D3 symmetry of water-soluble carboxylic acid C60 derivatives, containing three malonic acid groups per molecule, were synthesized and found to be equipotent free radical scavengers in solution as assessed by EPR analysis. Both compounds also inhibited the excitotoxic death of cultured cortical neurons induced by exposure to N-methyl-d-aspartate (NMDA), α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), or oxygen-glucose deprivation, but the C3 regioisomer was more effective than the D3 regioisomer, possibly reflecting its polar nature and attendant greater ability to enter lipid membranes. At 100 μM, the C3 derivative fully blocked even rapidly triggered, NMDA receptor-mediated toxicity, a form of toxicity with limited sensitivity to all other classes of free radical scavengers we have tested. The C3 derivative also reduced apoptotic neuronal death induced by either serum deprivation or exposure to Aβ1–42 protein. Furthermore, continuous infusion of the C3 derivative in a transgenic mouse carrying the human mutant (G93A) superoxide dismutase gene responsible for a form of familial amyotrophic lateral sclerosis, delayed both death and functional deterioration. These data suggest that polar carboxylic acid C60 derivatives may have attractive therapeutic properties in several acute or chronic neurodegenerative diseases.

https://www.pnas.org/content/pnas/94/17/9434.full.pdf

Carboxyfullerenes as neuroprotective agents

Effect of structural character of gold nanoparticles in nanofluid on heat pipe thermal performance

2. Formation of Aldehydes 3191 3. Formation of Ketones 3194 4. Formation of Silyl Enol Ethers 3194 C. Reductive Heck Reactions 3194 D. Miscellaneous Reactions 3196 III. R-Heteroatom-Substituted C−X Bond Activation 3197 A. Cross-Coupling Reactions 3197 1. Kumada−Corriu Reaction 3197 2. Stille Reaction 3197 3. Manganese-Catalyzed Reactions 3198 B. Carbonylation 3198 C. Reductive Carbonylation 3199 IV. Chelation Assisted Activation of a Proximal C−X Bond 3199

Transition metal-catalyzed activation of aliphatic C-x bonds in carbon-carbon bond formation.

A bright-blue electroluminescent device has been fabricated by using an emissive dopant and an electron-transporting host. The dopant was a highly photoluminescent silyl-substituted ter-(phenylene–vinylene) derivative [1,4-bis[4-(2-trimethylsilylvinly) styryl]-2,5-dibutoxybenzene (BTSB)]. BTSB was doped into a trimer of N-arylbenzimidazoles (TPBI) which functioned as the host and electron transporter. N,N′-bis-(1-naphthyl)-N,N′-diphenyl-1,1′-biphenyl-4-4′-diamine (NPB) was used as the hole transporter. The device, with a structure of indium tin oxide\NPB\TPBI:10%BTSB\TPBI\Mg:Ag, shows a bright blue emission of 11000 cd/m2 at a current density of 360 mA/cm2. The current efficiency of this device is about 3.2 cd/A at 20 mA/cm2.

Bright-blue electroluminescence from a silyl-substituted ter-(phenylene–vinylene) derivative

C60, vitamin E, and three C60 derivatives (polar 1 and water-soluble C3/D3C60s) were examined for their antioxidant effects on prevention of lipid peroxidation induced by superoxide and hydroxyl radicals The protection effect on lipid peroxidation was found to be in the sequence:  C60 ≥ vitamin E > 1 > none, for liposoluble antioxidants, and C3C60 ≫ D3C60 > none, for water-soluble ones Fluorescence quenching of PyCH2COOH (Py = pyrene) by both C3- and D3C60s shows that the Stern−Volmer constant, KSV, is about the same for both quenchers in aqueous solution Upon addition of liposomes, the fluorescence quenching becomes more efficient:  5-fold higher in KSV for C3C60 than for D3C60 When Py(CH2)nCOOH (n = 1, 3, 5, 9, or 15) was incorporated in lipid membranes, the KSVs all were small and nearly equal for D3C60 but were quite large and different for C3C60 with the sequence:  n = 1 < 3 < 5 < 9 < 15 The better protection effect of C3C60 on lipid peroxidation than that of D3C60 is attributed to its stronger 

Tien-Yau Luh

Papers

Carboxyfullerenes as neuroprotective agents

Effect of structural character of gold nanoparticles in nanofluid on heat pipe thermal performance

Transition metal-catalyzed activation of aliphatic C-x bonds in carbon-carbon bond formation.

Bright-blue electroluminescence from a silyl-substituted ter-(phenylene–vinylene) derivative

C60 and Water-Soluble Fullerene Derivatives as Antioxidants Against Radical-Initiated Lipid Peroxidation