排序方式: 共有13条查询结果,搜索用时 31 毫秒
1.
Dr. Longbin Ren Dr. Tullimilli Y. Gopalakrishna Dr. In-Hyeok Park Yi Han Prof. Jishan Wu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(6):2250-2254
We report the template-free synthesis and characterization of a new type of porphyrin/quinoidal-bithiophene-based conjugated macrocycle. X-ray crystallographic analysis of the dimer ( 2MC ) revealed a cyclophane-like geometry with large dihedral angles between the porphyrin and the neighboring thiophene rings, and NMR measurements and theoretical calculations confirmed a localized aromatic character of the porphyrin/thiophene rings and quinoidal character of the bithiophene linkers. Restricted rotation of the thiophene rings linked to the porphyrin unit was observed by variable-temperature NMR measurements. The dication ( 2MC2+ ) adopts a chair-shaped conformation to facilitate π-electron delocalization around the whole macrocycle. As a result, the molecule is globally aromatic, with a dominant 54 π conjugation pathway. The trimer ( 3MC ) also shows localized aromatic character of porphyrin rings and conformational flexibility, but its dication ( 3MC2+ ) is rigid and globally aromatic with a dominant 82 π conjugation pathway. 相似文献
2.
3.
Peng‐Fei Li Tyler B. Schon Dwight S. Seferos 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(32):9493-9498
3D frameworks are important because of their potential to combine the advantageous properties of porous materials with those associated with polymers. A series of novel 3D aromatic frameworks are presented that incorporate the heterocycles thiophene, selenophene, and tellurophene. The specific surface area and pore width of frameworks depends on the element that is used to build the framework. Optoelectronic properties are element‐dependent, with heavy atoms red‐shifting the optical properties and decreasing the energy gap of the solid. The metalloid nature of tellurophene allows the properties of this material to be tuned based on its oxidation state, even as an insoluble solid. The incorporation of the optoelectronic active thiophene, selenophene, and tellurophene units and the effect that they have on properties was studied. A supercapcitor device was fabricated using these frameworks, showing that these 3D frameworks are promising for optoelectronic uses. 相似文献
4.
The investigation of the dried roots of A. absinthium afforded two known lignans of tetrahydrofuran skeleton, sesamin and yangambin, one known coumarin, 6‐methoxy‐7,8‐methylenedioxy coumarin and a new thiophen acetylene. The structures were elucidated by spectroscopic methods. 相似文献
5.
A new one‐step synthesis of highly substituted thiophen‐2(3H)‐one derivatives was developed. 2‐Aryl‐1‐(morpholin‐4‐yl)ethanethiones were reacted with 2‐chloro‐2‐phenylacetyl chloride in DMF in the presence of a base to give the title compounds in moderate‐to‐good yields. 相似文献
6.
7.
8.
9.
Reaction between Furan‐ or Thiophene‐2‐carbonyl Chloride,Isocyanides, and Dialkyl Acetylenedicarboxylates: Multicomponent Synthesis of 2,2′‐Bifurans and 2‐(Thiophen‐2‐yl)furans 下载免费PDF全文
Mohammad Hosein Sayahi Mehdi Adib Zeinab Hamooleh Long‐Guan Zhu Massoud Amanlou 《Helvetica chimica acta》2015,98(9):1231-1239
An efficient multi‐component synthesis of highly functionalized 2,2′‐bifurans and 2‐(thiophen‐2‐yl)furans is described. A mixture of furan‐ or thiophene‐2‐carbonyl chloride, an isocyanide, and a dialkyl acetylenedicarboxylate undergoes a smooth addition reaction in dry CH2Cl2 at ambient temperature to produce 2‐amino‐5‐(4‐chlorofuran‐2‐yl)furan‐3,4‐dicarboxylates and 2‐amino‐5‐(4‐chlorothiophen‐2‐yl)furan‐3,4‐dicarboxylates. A single‐crystal X‐ray‐analysis of a derivative conclusively confirms the structure of these 2,2′‐bifurans and 2‐(thiophen‐2‐yl)furans. A novel electrophilic aromatic substitution reaction can justify the formation of the Cl‐substituted furan or thiophene rings. 相似文献
10.
Yong Ni Dr. Tullimilli Y. Gopalakrishna Shaofei Wu Prof. Jishan Wu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(19):7484-7488
A soluble and stable core-modified [38]octaphyrin, MC-T8 , containing eight thiophene rings was synthesized by Yamamoto coupling followed by oxidative dehydrogenation. X-ray crystallographic analysis revealed a nearly planar backbone, and the molecule is globally aromatic with a dominant 38π conjugation pathway. The dication MC-T82+ is antiaromatic, and the backbone is distorted, with a different orientation of the thiophene rings. The tetracation MC-T84+ becomes aromatic again, with a shallow-bowl-shaped geometry. Both the neutral compound and the dication demonstrated open-shell diradical character with a small singlet–triplet energy gap (−2.70 kcal mol−1 for MC-T8 and −3.78 kcal mol−1 for MC-T82+ ), and they are stable owing to effective spin delocalization. 相似文献