Enhancing electron affinity and tuning band gap in donor-acceptor organic semiconductors by benzothiadiazole directed C-H borylation.

Enhancing electron affinity and tuning band gap in donor-acceptor organic semiconductors by benzothiadiazole directed C-H borylation.

Item
http://www.wikidata.org/entity/Q44264845
Fully conjugated ladder polymers.Locking the Coplanar Conformation of π-Conjugated Molecules and Macromolecules Using Dynamic Noncovalent Bonds.Luminescent organoboron ladder compounds via directed electrophilic aromatic C-H borylation.Synthesis and optical and electrochemical properties of a phenanthrodithiophene (fused-bibenzo[c]thiophene) derivative.Enhancing thermally activated delayed fluorescence characteristics by intramolecular B-N coordination in a phenylpyridine-containing donor-acceptor π-system.Hydroboration as an Efficient Tool for the Preparation of Electronically and Structurally Diverse N→B-Heterocycles.Donor-Appended N,C-Chelate Organoboron Compounds: Influence of Donor Strength on Photochromic Behaviour.Highly Emissive Far Red/Near-IR Fluorophores Based on Borylated Fluorene-Benzothiadiazole Donor-Acceptor Materials.Synthesis and optical and electrochemical properties of julolidine-structured pyrido[3,4-b]indole dye.Air-Stable Spirofluorene-Containing Ladder-Type Bis(alkynyl)borane Compounds with Readily Tunable Full Color Emission Properties.Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons.Generation of an N→B Ladder-type Structure by Regioselective Hydroboration of an Alkenyl-Functionalized Quaterpyridine.Benzodipyrrole-based Donor-Acceptor-type Boron Complexes as Tunable Near-infrared-Absorbing Materials.A simple multi-responsive system based on aldehyde functionalized amino-boranes.A modular synthetic approach for band-gap engineering of armchair graphene nanoribbons.Four-coordinate triarylborane synthesis cascade B-Cl/C-B cross-metathesis and C-H bond borylationBN Embedded Polycyclic π-Conjugated Systems: Synthesis, Optoelectronic Properties, and Photovoltaic Applications
P2860

Enhancing electron affinity and tuning band gap in donor-acceptor organic semiconductors by benzothiadiazole directed C-H borylation.

Item
http://www.wikidata.org/entity/Q44264845
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Enhancing electron affinity an ...... azole directed C-H borylation.
@en
Enhancing electron affinity an ...... azole directed C-H borylation.
@nl
type
label
Enhancing electron affinity an ...... azole directed C-H borylation.
@en
Enhancing electron affinity an ...... azole directed C-H borylation.
@nl
prefLabel
Enhancing electron affinity an ...... azole directed C-H borylation.
@en
Enhancing electron affinity an ...... azole directed C-H borylation.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P921
P932
P356
P1433
P1476
Enhancing electron affinity an ...... azole directed C-H borylation.
@en
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P921
P932