functionalized helical building blocks (Nanoelectronics Research Corporation)
90
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Nanoelectronics Research Corporation
functionalized helical building blocks
Functionalized Helical Building Blocks, supplied by Nanoelectronics Research Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/functionalized+helical+building+blocks/functionalized+helical+building+blocks/pm40177945-193-13-19
Average 90 stars, based on 1 article reviews
Functionalized Helical Building Blocks, supplied by Nanoelectronics Research Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/functionalized+helical+building+blocks/functionalized+helical+building+blocks/pm40177945-193-13-19
Average 90 stars, based on 1 article reviews
functionalized helical building blocks - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: Chirality Amplified: Long, Discrete Helicene Nanoribbons. Article Snippet: Here we report the synthesis of two polyhelicene frameworks consisting, from end-to-end, of 18 and 24 fused benzene rings.. The latter exhibits the largest electronic circular dichroism in the visible spectrum of any molecule.. These shapepersistent helical nanoribbons incorporate multiple helicenes, a class of contorted polycyclic aromatic molecules consisting of ortho-annulated rings. Article Title: Regiochemically Pure 1,6-Ditriflato-Perylene Diimide: Preparation and Transformation. Article Snippet: Preparation of regioisomerically pure 1,6-disubstituted perylene diimide (PDI) is not a trivial task owing to the lack of facile synthetic and separation methodologies for the precursors.. Herein, we present a simple synthesis for 1,6-ditriflato-PDI (1,6-diOTf-PDI) using 1,6,9,10-tetrabromo-perylene monoimide 1 as the starting material.. The selective methoxylation of 1 at the 1,6-position is the key step. Article Title: High-Performance Organic Electronic Materials by Contorting Perylene Diimides. Article Snippet: Perylene diimide (PDI) is a workhorse of the organic electronics community.. However, the vast majority of designs that include PDI substitute the core with various functional groups to encourage intimate cofacial contacts between largely planar PDIs.. Over the past several years, we have observed the counterintuitive result that contorting the planar aromatic core of PDI leads to higher performing photovoltaics, photodetectors, batteries, and other organic electronic devices. Article Title: Regiochemically Pure 1,6-Ditriflato-Perylene Diimide: Preparation and Transformation. Article Snippet: (1) (a) Khokhlov, K.; Schuster, N. J.; Ng, F.; Nuckolls, Article Title: Green-Light Responsive Perylene Bisimides for Atom-Economic Thiol Generation and Click-Ligation. Article Snippet: [2] Khokhlov, K.; Schuster, N. J.; Ng, F.; Nuckolls, Article Title: Single-Handed Helicene Nanoribbons via Transfer of Chiral Information. Article Snippet: 1 Khokhlov, K.; Schuster, N. J.; Ng, F.; Nuckolls, Article Title: π-Conjugated redox-active two-dimensional polymers as organic cathode materials Article Snippet: (1) Khokhlov, K.; Schuster, N. J.; Ng, F.; Nuckolls, Article Title: Spin Filtering with Surface-Active Helicene- and Twistacene-Based Perylene Diimides. Article Snippet: Creating new chiral molecular and macromolecular systems that can polarize the spin of electrons has the dual promise of both applications in spintronics and a fundamental understanding of their origins.. Here, we put forward two optically active helical ladder dimers from perylene diimide-based twistacenes and helicenes.. We detail a scalable method to separate the helices for each of these systems and methods to functionalize them with thiol groups that allow for self-assembled monolayer formation on metal surfaces. |