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Universidad Nacional Autónoma de México - CNyN

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1st International Symposium on Nanoscience and Nanomaterials<br />

PLENARY VI<br />

SOLID-VACUUM, SOLID-GAS AND SOLID-LIQUID INTERFACES: STRUCTURE AND<br />

DYNAMICS UNDER ENVIRONMENTALLY RELEVANT CONDITIONS<br />

Miquel Salmeron<br />

Lawrence Berkeley National Laboratory and Materials Science and Engineering Dept.<br />

University of California at Berkeley.<br />

New revolutionary technologies are nee<strong>de</strong>d to produce clean and renewable energies, efficient and<br />

highly selective chemical processes (green catalysis), high capacity rechargeable batteries, and fuel cells and<br />

also to find solutions to environmental problems. For this it is imperative to <strong>de</strong>velop new fundamental<br />

approaches to the study of the interface of solid materials with gases, liquids and solids, because it is in these<br />

environments that crucial processes occur that need to be un<strong>de</strong>rstood to enable revolutionary discoveries. One<br />

way to control the structure of interfaces and their properties is through the <strong>de</strong>sign of materials of nanoscale<br />

dimensions, with specific shapes, size and compositions. It is also imperative to use techniques that make<br />

possible in situ atomic level structural and spectroscopic characterization of interfaces. Today we are entering<br />

a new era of interface science and technology as a result of novel technical <strong>de</strong>velopments. The experimental<br />

results obtained so far with some of the newly <strong>de</strong>veloped techniques are very promising and <strong>de</strong>monstrate that<br />

the goal of control and examination of the nanoscale properties of interfaces is within reach. I will illustrate<br />

this with examples from research carried out in my laboratory, using scanning tunneling microscopy (STM),<br />

and new photoelectron and x-ray absorption spectroscopies (PES) un<strong>de</strong>r ambient conditions. Applications to<br />

catalyst mo<strong>de</strong>ls, in the form of thin films, single crystals and nanoparticles will be examined for applications<br />

in catalysis and electrochemistry.<br />

PLENARY VII<br />

CATALYSIS AND COMPLEXITY IN NANOTECHNOLOGY:<br />

FROM MECHANISM TO FUNCTION<br />

Valery V. Fokin<br />

1 The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA<br />

fokin@scripps.edu<br />

Keywords: catalysis, organic synthesis, <strong>de</strong>ndrimers, click chemistry<br />

Nanotechnology, as a molecular science, <strong>de</strong>pends on the efficient methods for controlled and<br />

<strong>de</strong>pendable assembly of complex molecular architectures. These molecular architectures store and transmit<br />

information and, therefore, have a <strong>de</strong>sired function. To succeed in this molecular construction en<strong>de</strong>avor, one<br />

requires exquisitely selective chemical transformations that can reliably introduce various functional groups<br />

in the product. Catalysis is at the heart of chemistry and disciplines that directly <strong>de</strong>pend on it, for harnessing<br />

the complexity of catalytic processes offers unprece<strong>de</strong>nted potential for making them useful on both<br />

laboratory and industrial scales. Catalytic activation of alkynes with transition metals will be the central<br />

theme of the lecture. Alkynes are among the most energetic hydrocarbons, and transition metals enable<br />

selective and controlled manipulation of the triple bond, opening the door to the wealth of reliable reactivity:<br />

transformations of alkynes into heterocycles and into a variety of molecules with new carbon–heteroatom<br />

bonds. The combination of catalytic alkyne functionalization followed by manipulation of the resulting<br />

4

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