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Sylvain L. Gilat

Researcher at Bell Labs

Publications -  12
Citations -  2081

Sylvain L. Gilat is an academic researcher from Bell Labs. The author has contributed to research in topics: Photochromism & Dendrimer. The author has an hindex of 10, co-authored 12 publications receiving 2045 citations. Previous affiliations of Sylvain L. Gilat include University of California, Berkeley & Centre national de la recherche scientifique.

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Synthetic chemistry for ultrapure, processable, and high-mobility organic transistor semiconductors.

TL;DR: This Account reviews the synthetic methods that have been most useful for preparing a range of semiconductors, including thiophene-based oligomers, several kinds of fused rings, and polymers, and the tradeoff between process efficiency and target purity is emphasized.
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Light Harvesting and Energy Transfer in Laser-Dye-Labeled Poly(aryl ether) Dendrimers

TL;DR: The photophysical properties of a series of laser−dye-labeled poly(aryl ether) dendrimers, generations 1−4, have been determined and these macromolecules have the potential to become integral components of molecular photonic devices.
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Light harvesting and energy transfer in novel convergently constructed dendrimers

TL;DR: By the attachment of interacting laser dyes to the chain ends and focal point of a dendritic macromolecule it is possible to funnel energy harvested by the large peripheral antenna of the dendrimer efficiently and directly to the central fluorescent core by a process that does not involve the dendedrimer inner backbone.
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Light-triggered electrical and optical switching devices

TL;DR: The functional photoswitchable systems 1, 3 and 12-15 display pronounced photochromic properties; the bis-pyridinium derivative 1 represents a prototype of a switched molecular wire which may be converted from an open unconjugated form to a closed electron-conducting state as discussed by the authors.
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Photochemical pKa‐Modulation and Gated Photochromic Properties of a Novel Diarylethene Switch

TL;DR: The unsymmetrical dithienylethene photochrome 1a exhibits proton-gated photochromic properties as well as novel chemical reactivity as mentioned in this paper, and the dimethoxylated derivative 9a represents a light-triggered proton switch whose dissociation constant is increased by a factor of 16 upon photochemical cyclization to 9b.