Synthesis of Fullerene Hydrazine Derivatives

C 60 /C 70 mixture reacts with hydrazine hydrate catalysed by tetrabutylammonium bromide (TBAB) in the presence of air to afford fullerene hydrazine derivatives C 60 (OH) n(NHNH 2) n and C 70 (OH) n(NHNH 2) n,which are characterized by means of MS and FTIR.A possible reaction mechanism is discussed.

Use of Hydrazine and Its Substitutes as Fuel

Due to the properties and high reactivity of hydrazine,it is mainly used as rocket fuel not only in its pure form but also in combination with 1,1-dimethylhydrazine and oxidizers(nitrogen tetroxide or nitric acid)forming a self-igniting mixture with oxidizers.Aerozine 50 and UH 25(a mixture of 75%UDMH(unsymmetrical dimethylhydrazine)and 25%hydrazine hydrate)are the best-known hydrazine mixtures with different hydrazine concentrations.The review addresses the use of hydrazine and its derivatives as fuel.Hydrazine is employed in fuel cells(with air oxygen as an oxidizer)to generate electrochemical energy for transport vehicles.Hydrazine is widely used as monopropellant to design low-thrust rocket engines for orientation and stabilization systems in space vehicles,as well as in energy units.The review also addresses such hydrazine derivatives as methylhydrazine,1,1-dimethylhydrazine,hydrazine monoperchlorate,hydrazine diperchlorate,hydrazine diammonium tetraperchlorate,hydrazine mononitrate,hydrazine dinitrate,hydrazine nitroformate,hydrazine azides,tetrafluorohydrazine,etc.as well as composite propellants,and gel rocket propellants based on hydrazine.The materials in the review can be used as reference information on hydrazine fuels.

Fluoride-Responsive Organogel Based on Hydrazide Derivatives

An organogelator named N-[3-(hydroxy)-4-(dodecyloxy)-benzoyl]-N’ (4’-nitro-benzoyl) hydrazide (D12) was synthesized. It could form stable gels in some of the tested organic solvent. SEM images revealed that the molecules self- assembled into fibrous aggregates in the xerogels. The X-ray diffraction analysis showed that the xerogel exhibited a layered structure. FT-IR studies confirmed that intermolecular hydrogen bonding between C=O and N-H groups was the major driving force for gelation of organic solvents. The gel exhibited gel-sol transition and color change upon addition of F- . An extended conjugated system formed through the phenyl group and a five-membered ring based on intramolecular hydro-gen bonding between the oxygen atom near the deprotonation nitrogen atom and the other NH, which is responsible for the dramatic color change upon addition of F- .