Results 171 to 180 of about 9,278 (213)

Iontronic Click-to-Release Enables Electrically Controlled Delivery of Drugs and Biomolecules Beyond Charge and Size Limitations

Bintinger J, Hecko S, Vleugels M, Bayer C, Byun D, Hörberg M, Poremba N, Boukraa R, Keppel P, Löffler A, Kuba W, Schindl R, Waldherr L, Mikula H, Unemo HS, Bernacka-Wojcik I, Sjöström TA, Simon D, Berggren M.   +18 more
europepmc   +1 more source

Strong Magnetic Coupling and Single-Molecule Magnet Behavior in Tetrazinyl Radical-Bridged Metallocenes. [PDF]

Chemistry
Bajaj N, Mavragani N, Kitos AA, Gayfullina R, Moilanen JO, Murugesu M.   +5 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

The unknown unsubstituted tetrazines: 1,2,3,4-tetrazine and 1,2,3,5-tetrazine

The Journal of Organic Chemistry, 1991
Ab initio theoretical methods have been used to determine the equilibrium geometry of the unsubstituted 1,2,3,4- and 1,2,3,5-tetrazines. Double zeta (DZ) and double zeta plus polarization (DZP) basis sets have been used at both the self-consistent field (SCF) and single and double excitation configuration interaction (CISD) levels of theory.
J. Russell Thomas, Geoffrey E. Quelch, Henry F. Schaefer   +2 more
openaire   +1 more source

Tetrazine Explosives

Propellants, Explosives, Pyrotechnics, 2004
AbstractThe synthesis and properties of various 1,2,4,5‐tetrazine explosives and energetic materials are described. These are the nitrate and perchlorate salts of 3,6‐diguanidino‐1,2,4,5‐tetrazine, the nitrate and perchlorate salts of 3,6‐diguanidino‐1,2,4,5‐tetrazine‐1,4‐di‐N‐oxide, 3,6‐bis(1H‐1,2,3,4‐tetrazol‐5‐ylamino)‐1,2,4,5‐tetrazine and its 1,4 ...
David E. Chavez, Michael A. Hiskey, Darren L. Naud   +2 more
openaire   +1 more source

The photodissociation of s-tetrazine and dimethyl-s-tetrazine

Chemical Physics Letters, 1978
Abstract The photodissociation of s -tetrazine (ST) and its dimethyl derivative (DMST) has been investigated in hexane solutions at room temperature and in argon matrices and organic molecular crystals at cryogenic temperatures. Contrary to what has generally been assumed, only ST photodissociates upon excitation into its lowest excited singlet ...
D.M. Burland, F. Carmona, J. Pacansky
openaire   +1 more source

Synthesis of monosubstituted 1,2,4,5-tetrazines – 3-amino-1,2,4,5-tetrazines

Chemistry of Heterocyclic Compounds, 2017
The substitution of pyrazolyl moiety in 3-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazine with N-nucleophiles provided a series of highnitrogen tetrazine derivatives, including 2-nitro-1-(1,2,4,5-tetrazin-3-yl)guanidine, N-(1H-tetrazol-5-yl)-1,2,4,5-tetrazin-3-amine, N-(1,2,4,5-tetrazin-3-yl)-1,2,4,5-tetrazin-3-amine, N,N'-di(1,2,4,5-tetrazin-3-yl)-1 ...
Gennady F. Rudakov, Yurii A. Moiseenko, Natal’ya А. Spesivtseva   +2 more
openaire   +1 more source

Progress in 1,2,3,4-Tetrazine Chemistry

Chemical Reviews, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Aleksandr M, Churakov, Vladimir A, Tartakovsky   +1 more
openaire   +2 more sources

Selective Nucleophilic Substitutions on Tetrazines

HETEROCYCLES, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Novak, Z., Bostai, B., Csekei, M., Lorincz, K. A., Kotschy, A.   +4 more
openaire   +2 more sources

Acaricidal 1,2,4,5‐tetrazines

Pesticide Science, 1987
AbstractA series of 1,2,4,5‐tetrazines has been synthesised and screened for acaricidal activity. Laboratory tests have shown several of the compounds to be highly active mite ovicides. Further examination in the field has identified a highly active compound, which gives prolonged control of mites on top fruit.
Peter J. Brooker, John H. Parsons, Jim Reid, Peter J. West   +3 more
openaire   +1 more source

Triazines and Tetrazines

2014
Abstract This review covers the work published in the calendar year 2013. Novel reaction chemistry and new ring synthetic methods for 1,2,3-triazines, 1,2,4-triazines, 1,3,5-triazines, and tetrazines are reviewed.
Anton M. Prokhorov, Dmitry N. Kozhevnikov   +1 more
openaire   +1 more source