83204-68-6Relevant articles and documents
An effective and regioselective bromination of 1,4,5,8- naphthalenetetracarboxylic dianhydride using tribromoisocyanuric acid
Suseela,Sasikumar,Govindaraju
, p. 6314 - 6318 (2013)
A highly efficient and cost-effective reagent for the bromination of 1,4,5,8-naphthalenetetracarboxylic dianhydride under mild reaction conditions is reported. Bromination of 1,4,5,8-naphthalenetetracarboxylic dianhydride using tribromoisocyanuric acid (TBCA) in concentrated H2SO4 is very effective and regioselective. 1,4,5,8-Naphthalenetetracarboxylic dianhydride was brominated smoothly under optimized reaction conditions to give mono-, di- and tetra-brominated products in good to excellent yields using TBCA. As a proof of principle, the potential of this bromination methodology is demonstrated by converting brominated naphthalenetetracarboxylic dianhydrides into N-imide and core functionalized 1,4,5,8-napthalenetetracarboxylic diimides by treating with n-butylamine to yield corresponding mono-, di- and tetra-(n-butylamino)-naphthalene diimides in good yields in one-step reactions.
Quinoidization of π-Expanded Aromatic Diimides: Photophysics, Aromaticity, and Stability of the Novel Quinoidal Acenes
Ayitou, A. Jean-Luc,Jockusch, Steffen,Kamatham, Nareshbabu,Li, Jingbai,Rogachev, Andrey Yu.,Shokri, Siamak,Yang, Guang
, (2019)
We report the synthesis and photophysical characterization of π-expanded quinoidal triplet chromophores which exhibit attractive light-harvesting properties. The kinetic of the triplet excited state of quinoidal benzotetraphene 2 was found to be one order of magnitude higher than the lifetime of 3(1)* from the less conjugated parent chromophore 1. Furthermore, the evaluation of the optoelectronic properties indicates that π-expansion helps narrow the optoelectronic band gap, but the influence of the additional aromatic rings in the structure of 2 and 3 compromises the stability of the p-quinoidal ring. QDM 2 was isolated and fully characterized; however, it was found to rearomatize to a mixture of uncharacterized radical species.
Rod-like oligomers incorporating 2,6-dialkylamino core-substituted naphthalene diimide as acceptors for organic photovoltaic
Fernando, Roshan,Mao, Zhenghao,Sauvé, Geneviève
, p. 1683 - 1692 (2013)
Core-substituted naphthalene diimides (core-substituted NDIs) were incorporated into rod-like molecules and oligomers through reaction at the imide nitrogen positions. N,N′-Di(4-bromophenyl)-2,6-di(N-alkylamino)-1,4,5,8- naphthalenetetracarboxydiimide was synthesized in only three steps, and used as a versatile platform to prepare extended structures by reaction with thiophene substrates using Suzuki-coupling conditions. The optoelectronic properties of the new compounds were examined by UV/vis absorption spectroscopy, fluorescence spectroscopy, cyclic voltammetry and theoretical calculations. The imide substituents had little effect on the optical and electrochemical properties of core-substituted NDIs in solution. A bathochromic shift of the absorption was observed upon film formation, accompanied by quenching of fluorescence. These observations are consistent with increased inter-molecular interactions between core-substituted NDI moieties in the solid state. All compounds were tested in organic solar cells by blending with poly(3-hexylthiophene), and several showed a photovoltaic effect, demonstrating their potential as electron acceptors in organic solar cell. The best solar cell was observed for core-substituted NDI with 4-(thiophen-2-yl)phenyl imide substituents (5a), showing a power conversion efficiency of 0.57% and a large open circuit voltage of 0.87 V. This approach allows new structure-property relationship studies of non-fullerene acceptors in organic solar cells, where one can vary the imide substituent to optimize photovoltaic parameters while keeping the optical and electrochemical properties constant.
Fabrication of diverse nano-architectures through the self-assembly of a naphthalene diimide derivative bearing four carbamates
Wagalgave, Sopan M.,Ducla, Duong,Bhosale, Rajesh S.,Kobaisi, Mohammad Al,Jones, Lathe A.,Bhosale, Sidhanath V.,Bhosale, Sheshanath V.
, p. 6785 - 6793 (2018)
A naphthalene diimide (NDI) derivative bearing four carbamate groups (coded as: W2) was synthesised using a multistep strategy, and utilizing solvophobic effects, the self-assembly of this molecule was studied using solvent mixtures. Self-assembly led to a variety of controllable morphologies of supramolecular structures on both the micro and nanoscale. Nanobelts, nanospheres, nano-corals, microflowers and nanograss-like morphologies were obtained in DMF, MCH, CHCl3, THF, water and MeOH solvent mixtures. UV-vis absorption, fluorescence emission spectroscopy, FT-IR and XRD gave insight into the mode of aggregation of W2 in various solvents. The polarity of the solvent mixtures used directed the self-organisation of W2 by driving the π-π stacking interaction between NDI cores, and the H-bonding between the carbamate moieties. Our studies show that the solvent polarity guides the self-assembly process during solvent evaporation leading to the formation of supramolecular nano- and microstructures under ambient conditions.
Naphthalene diimides with improved solubility for visible light photoredox catalysis
Rei?, Barbara,Wagenknecht, Hans-Achim
, p. 2043 - 2051 (2019)
Five core-substituted naphthalene diimides bearing two dialkylamino groups were synthesized as potential visible light photoredox catalysts and characterized by methods of optical spectroscopy and electrochemistry in comparison with one unsubstituted naphthalene diimide as reference. The core-substituted naphthalene diimides differ by the alkyl groups at the imide nitrogens and at the nitrogens of the two substituents at the core in order to enhance their solubility in DMF and thereby enhance their photoredox catalytic potential. The 1-ethylpropyl group as rather short and branched alkyl substituent at the imide nitrogen and the n-propyl group as short and unbranched one at the core amines yielded the best solubilities. The electron-donating diaminoalkyl substituents together with the electron-deficient aromatic core of the naphthalene diimides increase the charge-transfer character of their photoexcited states and thus shift their absorption into the visible light (500-650 nm). The excited state reduction potential was estimated to be approximately +1.0 V (vs SCE) which is sufficient to photocatalyze typical organic reactions. The photoredox catalytic activity in the visible light range was tested by the α-alkylation of 1-octanal as benchmark reaction. Irradiations were performed with LEDs in the visible light range between 520 nm and 640 nm. The irradiation by visible light together with the use of an organic dye instead of a transition metal complex as photoredox catalyst improve the sustainability and make photoredox catalysis “greener”.
Red fluorescent zwitterionic naphthalenediimides with di/mono-benzimidazolium and a negatively-charged oxygen substituent
Gao, Ge,Han, Songyan,Liu, Yanhong,Wang, Chunqin,Wang, Tianbao,Zhang, Cheng,Zheng, Xuesong,Zhou, Linsen
supporting information, p. 9422 - 9425 (2021/09/22)
The C-H/C-X cross-coupling of a benzimidazolium salt with 2Br-NDI afforded two unprecedented zwitterionic NDIs with di/mono-benzimidazolium and an extra negatively-charged oxygen substituent. They exhibited intensified red fluorescence in polar solvents and negative solvatochromism due to an intramolecular charge transfer process, and could specifically label lysosomes and the endoplasmic reticulum in living A549 cells, respectively. They represent a rare case of NDI-derived ionic fluorophores.
Organic small molecule electron transport material based on naphthalimide unit and application thereof
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Paragraph 0121-0126; 0134-0139; 0146-0151; 0159-0164, (2021/07/17)
The invention provides an organic small molecule electron transport material based on a naphthalimide unit and application thereof, belongs to the field of organic photoelectric materials, and solves the problems that in the prior art, the quantum dot light-emitting diode device is few in electron transport material selection and poor in device stability. The chemical structure of the organic small molecule electron transport material contains a naphthalimide unit, and the organic small molecule electron transport material has the advantages that 1) the lowest unoccupied molecular orbital energy level is low, electron injection and transport in a QLED device are facilitated, the highest occupied molecular orbital energy level is low, hole injection in the QLED device can be blocked, and the above two aspects are beneficial for improving the electroluminescent efficiency of the QLED device; (2) the absorption spectrum is mainly not located in a visible light region and does not absorb light emitted by the light-emitting layer in the QLED device; and 3) the material has a rigid configuration, can inhibit crystallization of the material, is beneficial to processing in a QLED, and is beneficial to improving the stability of a QLED device.
