Results 221 to 230 of about 355,560 (277)

Mapping Immunity With Cutting-Edge Spatial Biology and Tissue Cytometry Innovations. [PDF]

MedComm (2020)
Cárdenas-Piedra L, Samuel SG, Mungenast F, Yasothkumar D, Ecker RC, Batra J.   +5 more
europepmc   +1 more source

Applications of Pharmacometrics in Antibody-Drug Conjugate Development. [PDF]

Pharmaceutics
Cheng X, Ji S, Lee Y, Dong H.
europepmc   +1 more source

Ultra-narrow donor-acceptor nanoribbons. [PDF]

Nat Commun
Lawrence J, Đorđević L, Bachtiger F, Pinfold H, Walker M, Lu J, Sosso GC, Bonifazi D, Costantini G.   +8 more
europepmc   +1 more source

Paclitaxel induced-mechanical hypersensitivity is associated with time-dependant pro-inflammatory galectin-3⁺ macrophages accumulation in the dorsal root ganglia. [PDF]

Neurobiol Pain
Zeboudj L, Malcangio M.
europepmc   +1 more source

Three-Dimensional Fully Conjugated Carbaporphyrin Cage

Journal of the American Chemical Society, 2018
A fully conjugated three-dimensional (3D) expanded carbaporphyrin (2) was prepared in a one-pot procedure that involves a [2+4] condensation reaction between a dibenzo[ g, p]chrysene-bearing tetrapyrrole precursor (1) and pentafluorobenzaldehyde, followed by oxidation.
Xian-Sheng Ke, Taeyeon Kim, Qing He, Vincent M. Lynch, Dongho Kim, Jonathan L. Sessler   +5 more
core   +5 more sources

Aromaticity in Fully π-Conjugated Multicyclic Macrocycles

Journal of the American Chemical Society, 2023
The research on aromaticity has mainly focused on monocyclic [n]annulene-like systems or polycyclic aromatic hydrocarbons. For fully π-conjugated multicyclic macrocycles (MMCs), the electronic coupling between the individual constitutional macrocycles would lead to unique electronic structures and aromaticity.
Longbin Ren, Yi Han, Xudong Hou, Yong Ni, Ya Zou, Tianyu Jiao, Jishan Wu   +6 more
openaire   +3 more sources

Linear fully conjugated meso-aryl pentapyrrins

Tetrahedron Letters, 2009
A meso-2,6-dichlorophenyl pentapyrrin was prepared using a modified method for dipyrrane synthesis followed by simple DDQ oxidation. The fully conjugated structures formed via redox inter-conversions were studied using crystallographic as well as observed and calculated spectral data.
Shin, JY, Hepperle, SS, Dolphin, D
openaire   +3 more sources

Aromaticity in Fully π-Conjugated Open-Cage Molecules

Journal of the American Chemical Society, 2022
Although aromaticity in 2D π-conjugated monocyclic and polycyclic molecules has been intensively studied, aromaticity in 3D fully π-conjugated molecular cages remains largely unexplored mainly due to the synthetic challenges. Herein, we report the facile synthesis of a π-conjugated molecular cage (1) containing four dimethylmethylene-bridged ...
Shaofei Wu, Yong Ni, Yi Han, Shan Xin, Xudong Hou, Jun Zhu, Zhengtao Li, Jishan Wu   +7 more
openaire   +3 more sources

A Fully Conjugated 3D Covalent Organic Framework Exhibiting Band‐like Transport with Ultrahigh Electron Mobility

Angewandte Chemie - International Edition, 2021
Although pi-conjugated two dimensional (2D) covalent organic frameworks (COFs) have been extensively reported, developing fully pi-conjugated 3D COFs is still an extremely difficult problem due to the lack of fully pi-conjugated 3D linkers. We synthesize
Shitao Wang, Mao Wang, Zexu Li
exaly   +2 more sources