Results 91 to 100 of about 25,345 (208)

Supramolecular Macrocyclic Iodine Adsorbents Enable Photothermally Stable Perovskite Solar Cells

Advanced Science
In this study, the design and synthesis of two novel diazapentacene‐based macrocycles (M3 and M4) is reported via a one‐pot Yamamoto coupling reaction. These macrocycles are constructed by π‐extension of a dihydrophenazine core, maintaining its excellent
Yue Wu, Wen Li, Shengzhong Li, Yan‐Fei Niu, Cuihong Wang, Hai‐Bo Yang, Xiao‐Li Zhao, Xiaodong Li, Junfeng Fang, Xueliang Shi   +9 more
doaj   +1 more source

Synthesis and crystal structures of 5,17-dibromo-26,28-dihydroxy-25,27-dipropynyloxycalix[4]arene, 5,17-dibromo-26,28-dipropoxy-25,27-dipropynyloxycalix[4]arene and 25,27-bis(2-azidoethoxy)-5,17-dibromo-26,28-dihydroxycalix[4]arene

Acta Crystallographica Section E: Crystallographic Communications
The calixarenes, 5,17-dibromo-26,28-dihydroxy-25,27-dipropynyloxycalix[4]arene (C34H26Br2O4, 1), 5,17-dibromo-26,28-dipropoxy-25,27-dipropynyloxycalix[4]arene (C40H38Br2O4, 2) and 25,27-bis(2-azidoethoxy)-5,17-dibromo-26,28-dihydroxycalix[4]arene ...
Alexander Gorbunov, Stanislav Bezzubov, Maria Malakhova, Vladimir Kovalev, Ivan Vatsouro   +4 more
doaj   +1 more source

42-and 46-membered phosphorus-based macrocycles

, 2007
42- and 46-Membered phosphorus-based macrocycles were obtained in a [2+2] condensation of PhP(O)[N(Me)NH2]2 with dialdehydes. These macrocycles were isolated in a pure form after preparative thin layer chromatography and were characterized by ...
Pandian, Balasubramanian Murugesa, Andavan, Gurusamy Thangavelu Senthil, Chandrasekhar, Vadapalli, Azhakar, Ramachandran   +3 more
core   +1 more source

On-oligonucleotide olefin metathesis in water

Nature Communications
Genetically-encoded libraries represent a breakthrough in the large-scale screening of chemical matter. Within such technologies, encoded libraries of synthetic macrocycles generated by ring-closing metathesis hold significant potential to address ...
Chun Zhang, Christian O. Blanco, Anastasiya Khimich, Deryn E. Fogg, Andreas Brunschweiger   +4 more
doaj   +1 more source

Macrocycles

Drug Discovery Today: Technologies, 2018
Macrocycles are an emerging and largely underexploited part of chemical space where potential drugs for difficult genomic targets can be discovered. Macrocycles can have advantages over their natural twins such as better control over synthesis, physicochemical properties and target binding.
Abdelraheem, Eman M.M., Shaabani, Shabnam, Dömling, Alexander   +2 more
openaire   +1 more source

Engineering amino acid-derived Au(III) macrocycles as bioactive chemical biology agents. [PDF]

J Inorg Biochem
Holmes JC, Smith BC, Obisesan OA, Awuah SG.   +3 more
europepmc   +1 more source

RingKin: portraying the vast macrocyclic chemical universe surrounding kinase drugs. [PDF]

Chem Sci
Diao Y, Hu F, Jiang W, Hu Y, Ma S, Wu D, Tong L, Xiang S, Chen C, Li Z, Shen Z, Zhao Z, Xu Y, Li J, Li H.   +14 more
europepmc   +1 more source

Perfluorooctanesulfonate detection and removal with simple imidazolium macrocycles. [PDF]

Chem Sci
Garcia AC, Lian R, Paul SK, Jin X, Seth A, Venkatesan S, Zhang H, Yang YD, Awan M, Antony Benedict PS, Rajasekaran V, Carta V, Sessler JL, Siepmann JI, Hooley RJ.   +14 more
europepmc   +1 more source

Macrocyclic colibactins

Nature Chemistry, 2020
openaire   +3 more sources

Unveiling Mechanisms of Chlorinated Volatile Organic Compounds (CVOCs) and 1,4-Dioxane Sorption in Macrocyclic Materials: A DFT, MD, and Experimental Study. [PDF]

Langmuir
Patyal AS, Hana G, Sun Y, Shen Y, Howe JD.   +4 more
europepmc   +1 more source