Results 31 to 40 of about 630 (149)
Indandiazocines: Unidirectional molecular switches
We report theoretical investigations on azobenzene-based indandiazocines, novel chiral systems that perform unidirectional cis↔trans isomerizations upon photo-excitation. For three different systems of this kind, we have simulated excited-state surface-
Bernd Hartke, Tim Raeker
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Amine-Substituted Diazocine Derivatives – Synthesis, Structure, and Photophysical Properties [PDF]
A series of amine‐substituted diazocines were synthesized in three steps from methyl 2‐aminobenzoate or methyl 3‐aminonaphtholate. The saddle‐shaped diazocine compounds showed similar interplane angle of 75° despite the different steric bulk of the amine
White, JM +11 more
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Triplet-Sensitized Bidirectional Isomerization of Bridged Azobenzene [PDF]
Diazocine is a bridged azobenzene with both phenyl rings connected by a CH2-CH2 group. Despite this rather small structural difference, diazocine exhibits improved properties over azobenzene as a photoswitch, such as high switching efficiencies, very ...
Jussi, Isokuortti +7 more
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6H,12H-5,11-Ethanodibenzo[b,f][1,5]diazocine
In the molecule of the title compound, C16H16N2, the ethano-strapped analogue of unsubstituted Tröger's base, the dihedral angle between the two benzene rings is 75.85 (4)°, the smallest angle measured for an ethano-strapped analogue.
Peter Turner +2 more
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$E$-Diazocine in Chemical Education: Synthesis, Structure, Photochromism and Thermal Stability
Z‐diazocine, synthesized as described by Tellkamp,1 has been photochemically converted into E‐diazocine by irradiation of its solution at λ=365 nm. After purification, single crystals of E‐diazocine were obtained by recrystallization at −18 °C from n ...
Lehmann, C. +14 more
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Methods for facile synthesis of symmetric and unsymmetric functionalized analogues of Tröger's base were developed with use of 2,8-dibromo-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocine (2) as the starting material.
Jacob Jensen +9 more
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Synthesis of mono-functionalized S-diazocines via intramolecular Baeyer–Mills reactions
Herein we report a reliable method to synthesize mono-functionalized S-diazocines in reproducible yields via intramolecular Baeyer–Mills reactions. Diazocines exhibit excellent photoswitchable properties. As opposed to azobenzenes they are more stable in
Miriam Schehr +4 more
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Design and Synthesis of a Novel Banana-Shaped Functional Molecule via Double Cross-Coupling
A novel banana-shaped molecule using 2,8-Dimethyl-6H,12H-5,11-methanodibenzo [b,f] [1,5]diazocine (Tröger’s base) as bent-core was synthesized via double Carbon-Carbon cross-coupling reaction. The double Sonogashira cross-coupling reaction was
Bingchuan Yang +3 more
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2,8-Dimesitylboranyl-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocine
In the title compound, C51H56B2N2, a substituted Tröger's base, the dihedral angle between the two benzene rings constituting the Tröger's base framework is 104.42 (6)°.
Chun-Xue Yuan
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The title compound, C22H18N2O12, was obtained as a by-product during the planned synthesis of 1,2-bis(2-nitro-4,5-dimethyl phthalate)ethane by oxidative dimerization starting from dimethyl-4-methyl-5-nitro phthalate.
Artjom Businski +4 more
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