Zobrazeno 1 - 10
of 1 036
pro vyhledávání: '"M. Shreeve"'
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-8 (2023)
Abstract A primary explosive is an ideal chemical substance for performing ignition in military and commercial applications. For over 150 years, nearly all of the developed primary explosives have suffered from various issues, such as troublesome syn
Externí odkaz:
https://doaj.org/article/52b19910e37241e78daca5e4a7824e87
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-10 (2022)
Size matching molecular design utilizing host-guest chemistry is a general and promising strategy for seeking new functional materials. Here the authors screen different sized nitrogen rich azoles for selective encapsulation into a hydroxylammonium f
Externí odkaz:
https://doaj.org/article/6ff919a091e840249b417c00cc842e39
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-7 (2021)
Nitroformate is an attractive oxidant compound in propellants and explosives but its poor thermostability prevents it from application. Here, the authors demonstrate that incorporation of nitroformate in a hydrogen-bonded organic framework increases
Externí odkaz:
https://doaj.org/article/66039306dbdf46aa96b3bd35ef5701af
Publikováno v:
Energetic Materials Frontiers, Vol 1, Iss 1, Pp 2-15 (2020)
The research focus of studies on energetic salts has been to achieve targeted synthesis, structure and performance through modification of the organic anion and cation by addition of functional groups. In this review, the development direction and tr
Externí odkaz:
https://doaj.org/article/8f8ce593dd6c4701a3c5555282da4125
Autor:
Jichuan Zhang, Yongan Feng, Yiyang Bo, Ajay Kumar Chinnam, Jatinder Singh, Richard J. Staples, Xiaohui He, Kun Wang, Jiaheng Zhang, Jean’ne M. Shreeve
Publikováno v:
Chem. 8:2678-2687
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7129157cd1db6bcb75fb505fe90a20b
https://doi.org/10.1016/j.chempr.2022.06.007
https://doi.org/10.1016/j.chempr.2022.06.007
Publikováno v:
Journal of Materials Chemistry A. 10:8268-8272
A facile and efficient radical-mediated C–N bond activation method in a monocyclic pyrazole at room temperature was developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe08ac40debd95774fd07d520f051acb
https://doi.org/10.1039/d2ta01146h
https://doi.org/10.1039/d2ta01146h
Publikováno v:
Dalton Transactions. 51:17987-17993
Nitration of fused [1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7-diamine gives new stable and insensitive fused ring nitramine derivatives as a function of nitric acid concentration.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0b03c001b87719c4909f9750deb688b
https://doi.org/10.1039/d2dt03255d
https://doi.org/10.1039/d2dt03255d
Autor:
Elizabeth R, Woods, Susan J, Sommer, Emily A, Bryson, Kyra M, Shreeve, Dionne, Graham, Shari, Nethersole, Urmi, Bhaumik
Publikováno v:
Journal of Asthma. 59:2258-2266
To provide a 10-year follow-up of asthma cost-savings for patients served by the Community Asthma Initiative (CAI) group compared to a coarsely cost-matched comparison group from similar neighborhoods (comparison group).CAI provided home visits and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4461d7a9305c3bd8a6473e846466a2e
https://doi.org/10.1080/02770903.2021.2010746
https://doi.org/10.1080/02770903.2021.2010746
Publikováno v:
Organic Letters. 23:9408-9412
Structural binary cleavage of 3,7-diamino-2,6-dinitro-1H,5H-pyrazolo-[1,2-a]pyrazole-1,5-dione 3, under nucleophilic conditions, leads to the formation of a monocyclic pyrazole unit of 5-amino-4-nitro-1,2-dihydro-3H-pyrazol-3-one, 4. Additionally, va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0c5add66f339397ea41a20caf36e505
https://doi.org/10.1021/acs.orglett.1c03534
https://doi.org/10.1021/acs.orglett.1c03534