Results 71 to 80 of about 3,457 (229)
Herein, a selective, one‐pot synthetic route to reactive benzyl‐ and allyl‐halide‐substituted naphthalenes and dihydronaphthalenes from easily accessible 2,3‐aryl‐1,3‐butadiene substrates and simple halogenated alkanes, using [Cp*RuCl(PPh3)2] as the ...
Nicole S. van Leeuwen +9 more
doaj +1 more source
Naphthalenes Image microwave irradiation induced rearrangement on montmorillonite K-10
Irradiation of 4-aryl-4-alkylhex-5-en-2-ones (e.g. 1a) or 5-aryl-4-alkylhex-5-en-2-ones (e.g. 2a) adsorbed on montmorillonite K-10 in a commercial microwave oven furnishes the multialkylated naphthalenes (e.g. 3)
Srikrishna, A +3 more
core +1 more source
Increasing the frequency at which organic electronics operate while limiting the operation voltage is key to enabling future sustainable wireless applications. This work shows p‐type organic field‐effect transistors based on a molecularly doped, small molecule/polymer blend (C8‐BTBT:C16IDT‐BT), fabricated via direct‐writing and solution‐processing ...
Tommaso Losi +8 more
wiley +1 more source
Facile synthesis of asymmetric fluorinated spiro‐type HTMs combined with blade‐coating fabrication and vacuum‐assisted crystallization enables high‐efficiency PSCs with PCEs of 24.49% (0.09 cm2) and 23.28% (1.00 cm2), along with excellent stability.
Kun‐Mu Lee +13 more
wiley +1 more source
Iodophor-Catalyzed Disulfenylation of Amino Naphthalenes with Aryl Sulfonyl Hydrazines
An iodophor-catalyzed direct disulfenylation of amino naphthalenes with aryl sulfonyl hydrazines in water was developed. A series of aryl sulfides were obtained in moderate to excellent yields.
Yutong Yuan +4 more
doaj +1 more source
Internal reactions of ion/molecule complexes from isomeric protonated formyl-and acetyl-naphthalenes [PDF]
Filges U, Grützmacher H-F. Internal reactions of ion/molecule complexes from isomeric protonated formyl-and acetyl-naphthalenes. International Journal of Mass Spectrometry and Ion Processes.
Hans-Friedrich Grützmacher +3 more
core +1 more source
Permanent oxidative dipole (POD) engineering overcomes the electronic uniformity of quinoline‐linked COFs. By enhancing the dipole moment to 2.08 D and lowering exciton binding energy to 20.3 meV, it constructs a robust built‐in electric field and spatially decoupled redox centers. This bypasses inherent kinetic bottlenecks, achieving a 4569 µmol g−1 h−
Yong‐Quan Wu +2 more
wiley +1 more source
Polychlorinated naphthalenes (PCNs) are organochlorine compounds comprising the naphthalene ring system, in which one to eight hydrogen atoms have been substituted with chlorine atoms, yielding 75 chlorinated congeners.
Idowu Victoria Agunbiade +3 more
doaj +1 more source
Unlocking Li/Mg‐Based Photochemical Nitration Platforms for Anticancer Drug Discovery
Two low‐toxicity light main‐group metal photochemical systems based on lithium and magnesium are constructed for selective C(sp2)‐H (di)nitration of anilines. The obtained dinitrated products exhibit anti‐HCC (hepatocellular carcinoma) and anti‐KYSE30 cell activities, holding promise as novel antitumor candidates.
Qian Wan +13 more
wiley +1 more source
31P solid‐state nuclear magnetic resonance analysis revealed the presence of aluminum tripolyphosphate on the surface of a platinum/aluminum condensed phosphate mixture (ACPM) catalyst. This finding led to the development of a Pt/aluminum tripolyphosphate (Pt/ATPP) catalyst for the selective hydrogenolysis of phenols to arenes.
Kento Oshida +11 more
wiley +2 more sources

