scholarly journals Colored Janus Nanocylinders Driven by Supramolecular Coassembly of Donor and Acceptor Building Blocks

ACS Nano ◽  
2021 ◽  
Vol 15 (2) ◽  
pp. 2569-2577
Author(s):  
Thomas Choisnet ◽  
David Canevet ◽  
Marc Sallé ◽  
Cédric Lorthioir ◽  
Laurent Bouteiller ◽  
...  
2016 ◽  
Vol 3 (5) ◽  
pp. 545-555 ◽  
Author(s):  
Agnieszka Nowak-Król ◽  
Reinhard Wagener ◽  
Felix Kraus ◽  
Amaresh Mishra ◽  
Peter Bäuerle ◽  
...  

By variation of donor and acceptor building blocks in acceptor–donor–acceptor dyes a transition from p- to n-type semiconductor has been achieved.


2014 ◽  
Vol 69 (1) ◽  
pp. 98-102 ◽  
Author(s):  
Ahmed Bari

Monosaccharidic push-pull butadienes are interesting building blocks for the synthesis of various heterocyclic and natural products due to their biological prevalence and significant p-electron interactions between donor and acceptor groups. A series of 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy- 2-formyl-D-arabino-hex-1-enitol (2) and 1,5-anhydro-3,4-di-O-benzyl-2-deoxy-2-formyl-L-erythrohex- 1-enitol (4) derived push-pull branched chain sugars have been synthesized by condensation with active methylene compounds using basic aluminum oxide (Al2O3) or anhydrous sodium acetate (NaOAc) at room temperature. The compounds have been fully characterized by spectroscopic techniques and elemental analyses.


2014 ◽  
Vol 2 (41) ◽  
pp. 8651-8661 ◽  
Author(s):  
Yinghui He ◽  
Wei Hong ◽  
Yuning Li

This article reviews novel electron donor and acceptor building blocks for constructing π-conjugated polymers for organic thin film transistors and organic photovoltaics.


2014 ◽  
Vol 70 (a1) ◽  
pp. C638-C638
Author(s):  
Aouaouche Benkanoun ◽  
Fadéla Balegroune ◽  
Achoura Guehria-Laidoudi ◽  
Slimane Dahaoui ◽  
Claude Lecomte

The main strategy for preparing novel multifunctional materials is based on self-assembly method which employs polydentate organic ligands containing N- or O-donor as building blocks. In this context, those ligands like imidazole or carboxylate groups are of special interest due to their good coordination ability and diverse coordination modes [1]. As a part of our investigations of extended structures with mixed ligands, new complexes [Co(Hipht)2(Im)2(H2O)2] and [Co(Tpht)(Im)3(H2O)2].H2O were obtained by direct method, then characterized by IR spectroscopy, TG/ATD and X-ray crystallography. In the compound [Co(Hipht)2(Im)2(H2O)2], CoII is located on a symmetry center, surrounded by two aqua ligands, two hydrogeno-isophthalate ligands and two imidazole molecules, where all ligands adopt monodentate mode. The complex's geometry consist of two intermolecular N-H...O bonds (2,157 Å and 2,630 Å) formed by one H atom of imidazole ligand and oxygen atoms of acid molecules evolving along two directions, giving rise to R24 (16) synthons. The interplanar distance of 3,718 Å between two parallel imidazole rings reveals the existence of Π-Π interactions. In the [Co(Tpht)(Im)3(H2O)2].H2O [2], the Co cation exhibits an octahedral coordination sphere, with two aqua, three N-coordinated imidazole ligands and one terephthalato dianion. The three independent imidazole groups and the single terephtalate dianion, all unidentate participate respectively as donor and acceptor in strong to moderate hydrogen bonds, and allow the recognition of supramolecular dimensionality. The backbone of the architecture is the helical hydrogen-bonded ladder running along b axis, composed of alternating R44(10) and R33(8) heterosynthons, which are developed in bicyclic sheets. Non covalent interactions play a significant role in this class of materials [3], in fact, extended hydrogen bonds networks associated to Π-Π interactions lead to 3D supramolecular architecture for the two complexes.


2017 ◽  
Vol 13 ◽  
pp. 2094-2114 ◽  
Author(s):  
Weizhun Yang ◽  
Bo Yang ◽  
Sherif Ramadan ◽  
Xuefei Huang

Most glycosylation reactions are performed by mixing the glycosyl donor and acceptor together followed by the addition of a promoter. While many oligosaccharides have been synthesized successfully using this premixed strategy, extensive protective group manipulation and aglycon adjustment often need to be performed on oligosaccharide intermediates, which lower the overall synthetic efficiency. Preactivation-based glycosylation refers to strategies where the glycosyl donor is activated by a promoter in the absence of an acceptor. The subsequent acceptor addition then leads to the formation of the glycoside product. As donor activation and glycosylation are carried out in two distinct steps, unique chemoselectivities can be obtained. Successful glycosylation can be performed independent of anomeric reactivities of the building blocks. In addition, one-pot protocols have been developed that have enabled multiple-step glycosylations in the same reaction flask without the need for intermediate purification. Complex glycans containing both 1,2-cis and 1,2-trans linkages, branched oligosaccharides, uronic acids, sialic acids, modifications such as sulfate esters and deoxy glycosides have been successfully synthesized. The preactivation-based chemoselective glycosylation is a powerful strategy for oligosaccharide assembly complementing the more traditional premixed method.


CrystEngComm ◽  
2018 ◽  
Vol 20 (38) ◽  
pp. 5663-5666 ◽  
Author(s):  
Jia Huang ◽  
Jie Zhang ◽  
Runhua He ◽  
Zhiyong Fu

A novel Cd(ii)-MOF with tunable photophysical behavior has been developed. The control of color, fluorescence emission and conductivity is achieved in a single crystalline conductance switch by incorporating donor and acceptor building blocks into a molecular wire.


2021 ◽  
Author(s):  
Qi Sun

Organic molecules with large gap between the excited singlet/triplet states can be applied in hot exciton emission and singlet fission to beat the spin statistics limit in optoelectronic devices. Herein, a novel strategy is proposed for achieving large triplet-triplet gap (E(T1T2)) and singlet-triplet gap (E(S1T1)) by manipulating the aromaticity of the low-lying excited states. Partially conjugated five-membered heterocyclic rings are found to naturally have low E(T1) owing to high aromaticity obeying Baird’s Rule. Utilizing such ring (pyrazoline) as a bridge and selecting various donor and acceptor moieties, numbers of derivatives have been theoretically designed with tunable emission colors, significantly large E(T1T2) and E(S1T1), and satisfying E(T2)>E(S1)≥2E(T1). The ultrafast spectroscopy and sensitization measurements for one of them with blue fluorescence (named TPA-DBPrz) confirm the calculated prediction. This work opens a new avenue and provides molecular units to develop high-efficiency optoelectronic materials.


Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1652
Author(s):  
Mohamed M. H. Desoky ◽  
Matteo Bonomo ◽  
Nadia Barbero ◽  
Guido Viscardi ◽  
Claudia Barolo ◽  
...  

Perovskite solar cells are a hot topic of photovoltaic research, reaching, in few years, an impressive efficiency (25.5%), but their long-term stability still needs to be addressed for industrial production. One of the most sizeable reasons for instability is the doping of the Hole Transporting Material (HTM), being the salt commonly employed as a vector bringing moisture in contact with perovskite film and destroying it. With this respect, the research focused on new and stable “dopant-free” HTMs, which are inherently conductive, being able to effectively work without any addition of dopants. Notwithstanding, they show impressive efficiency and stability results. The dopant-free polymers, often made of alternated donor and acceptor cores, have properties, namely the filming ability, the molecular weight tunability, the stacking and packing peculiarities, and high hole mobility in absence of any dopant, that make them very attractive and a real innovation in the field. In this review, we tried our best to collect all the dopant-free polymeric HTMs known so far in the perovskite solar cells field, providing a brief historical introduction, followed by the classification and analysis of the polymeric structures, based on their building blocks, trying to find structure–activity relationships whenever possible. The research is still increasing and a very simple polymer (PFDT–2F–COOH) approaches PCE = 22% while some more complex ones overcome 22%, up to 22.41% (PPY2).


1997 ◽  
Vol 161 ◽  
pp. 23-47 ◽  
Author(s):  
Louis J. Allamandola ◽  
Max P. Bernstein ◽  
Scott A. Sandford

AbstractInfrared observations, combined with realistic laboratory simulations, have revolutionized our understanding of interstellar ice and dust, the building blocks of comets. Since comets are thought to be a major source of the volatiles on the primative earth, their organic inventory is of central importance to questions concerning the origin of life. Ices in molecular clouds contain the very simple molecules H2O, CH3OH, CO, CO2, CH4, H2, and probably some NH3and H2CO, as well as more complex species including nitriles, ketones, and esters. The evidence for these, as well as carbonrich materials such as polycyclic aromatic hydrocarbons (PAHs), microdiamonds, and amorphous carbon is briefly reviewed. This is followed by a detailed summary of interstellar/precometary ice photochemical evolution based on laboratory studies of realistic polar ice analogs. Ultraviolet photolysis of these ices produces H2, H2CO, CO2, CO, CH4, HCO, and the moderately complex organic molecules: CH3CH2OH (ethanol), HC(= O)NH2(formamide), CH3C(= O)NH2(acetamide), R-CN (nitriles), and hexamethylenetetramine (HMT, C6H12N4), as well as more complex species including polyoxymethylene and related species (POMs), amides, and ketones. The ready formation of these organic species from simple starting mixtures, the ice chemistry that ensues when these ices are mildly warmed, plus the observation that the more complex refractory photoproducts show lipid-like behavior and readily self organize into droplets upon exposure to liquid water suggest that comets may have played an important role in the origin of life.


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