The development of future quantum devices such as the maser, i.e., the microwave analog of the laser, could be well-served by the exploration of chemically tunable organic materials. Current iterations of room-temperature organic solid-state masers are composed of an inert host material that is doped with a spin-active molecule. In this work, we systematically modulated the structure of three nitrogen-substituted tetracene derivatives to augment their photoexcited spin dynamics and then evaluated their potential as novel maser gain media by optical, computational, and electronic paramagnetic resonance (EPR) spectroscopy. To facilitate these investigations, we adopted an organic glass former, 1,3,5-tri(1-naphthyl)benzene to act as a universal host. These chemical modifications impacted the rates of intersystem crossing, triplet spin polarization, triplet decay, and spin-lattice relaxation, leading to significant consequences on the conditions required to surpass the maser threshold.
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http://dx.doi.org/10.1021/acs.chemmater.3c00640 | DOI Listing |
Chemistry
November 2024
School of Chemistry and Chemical Engineering, Anhui University, 111 Jiulong Road, Hefei, Anhui, China.
RSC Adv
September 2024
Department of Materials Science and Engineering, University of California, Irvine Irvine CA 92697 USA
Acenes and -heteroacenes have been synthesized and studied for over a century because of their fundamentally interesting materials properties and promise for device applications. Within this context, our laboratory has previously synthesized nitrogen-containing tetrabenzo[,,,]pentacenes an aza-Diels-Alder reaction-based approach, and herein, we expand our methodology to obtain substituted, expanded, functionalized, and dimeric tetrabenzoacenes. Overall, our study adds to the limited number of tetrabenzoacene derivatives reported to date and may open further opportunities for these materials in organic optoelectronics applications.
View Article and Find Full Text PDFBeilstein J Org Chem
May 2024
Department of Chemistry, University of Florida, PO Box 117200, Gainesville, FL, 32611, United States.
Presented here is the design, synthesis, and study of a variety of novel hydrogen-bonding-capable π-conjugated -heteroacenes, 1,4-dihydropyrazino[2,3-]quinoxaline-2,3-diones (DPQDs). The DPQDs were accessed from the corresponding weakly hydrogen-bonding dicyanopyrazinoquinoxaline (DCPQ) suspensions with excess potassium hydroxide, resulting in moderate to good yields. Both families of compounds were analyzed by UV-vis and NMR spectroscopy, where the consequences of hydrogen bonding capability could be assessed through the structure-property studies.
View Article and Find Full Text PDFChem Mater
June 2023
Department of Materials, Imperial College London, South Kensington Campus, Exhibition Road, London SW7 2AZ, U.K.
The development of future quantum devices such as the maser, i.e., the microwave analog of the laser, could be well-served by the exploration of chemically tunable organic materials.
View Article and Find Full Text PDFChem Sci
October 2022
Department of Chemistry, Texas A&M University at Qatar P.O. Box 23874 Doha Qatar
Ladder-type thiazole-fused ,-heteroacenes with an extended π-conjugation consisting of six (SN6-Tz) and nine (SN9-Tz) fused aromatic rings have been synthesized and fully characterized. To date, the synthesis of well-defined fused building blocks and polymers of π-conjugated organic compounds based on the thiazole moiety is a considerable synthetic challenge, due to the difficulty in their synthesis. Acceptor-donor building blocks M1 and M2 were successfully polymerized into ladder homopolymers P1-P2 and further copolymerized with a diketopyrrolopyrrole unit to afford step-ladder copolymer P3.
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