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1.
Micromachines (Basel) ; 14(3)2023 Mar 09.
Artigo em Inglês | MEDLINE | ID: mdl-36985034

RESUMO

Multiband terahertz (THz) detectors show great application potential in imaging, spectroscopy, and sensing fields. Thermal detectors have become a promising choice because they could sense THz radiations on the whole spectrum. This paper demonstrates the operation principle, module designs with in-depth theoretical analysis, and experimental validation of a room-temperature CMOS monolithic resonant triple-band THz thermal detector. The detector, which consists of a compact triple-band octagonal ring antenna and a sensitive proportional to absolute temperature (PTAT) sensor, has virtues of room-temperature operation, low cost, easy integration, and mass production. Good experimental results are obtained at 0.91 THz, 2.58 THz, and 4.2 THz with maximum responsivities of 32.6 V/W, 43.2 V/W, and 40 V/W, respectively, as well as NEPs of 1.28 µW/Hz0.5, 2.19 µW/Hz0.5, and 2.37 µW/Hz0.5, respectively, providing great potential for multiband THz sensing and imaging systems.

2.
Org Lett ; 24(37): 6783-6788, 2022 09 23.
Artigo em Inglês | MEDLINE | ID: mdl-36074995

RESUMO

The cascade of Ir-catalyzed enantioselective allylic amination and Cu-catalyzed alkyne-azide cycloaddition was designed for the asymmetric synthesis of homoallylic amidines. The nucleophilic addition of an in situ-generated enantioenriched tertiary allylamine to a ketenimine intermediate triggers a rapid and stereospecific zwitterionic aza-Claisen rearrangement in a 1,3-chiral transfer manner. The approach allows modular access to enantioenriched α-chiral homoallylic amidines in high yields with a high level of enantiomeric purity.


Assuntos
Alilamina , Amidinas , Alcinos , Azidas , Catálise , Estrutura Molecular
3.
Org Lett ; 22(8): 3234-3238, 2020 Apr 17.
Artigo em Inglês | MEDLINE | ID: mdl-32233500

RESUMO

A copper-catalyzed three-component reaction of terminal alkynes, TsN3, and tertiary allylic amines is developed toward the one-pot synthesis of α-allylic amidines. The product was synthesized on gram scale under 1 mol % of catalyst loading. Transformations of products into alkenyl amine and other nitrogen-containing compounds are demonstrated without any loss of stereochemical information.

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