Abstract:
Amines and amine derivatives that improve the buffering range, and/or reduce the chelation and other negative interactions of the buffer and the system to be buffered. The reaction of amines or polyamines with various molecules to form polyamines with differing pKa's will extend the buffering range, derivatives that result in polyamines that have the same pKa yields a greater buffering capacity. Derivatives that result in zwitterionic buffers improve yield by allowing a greater range of stability.
Abstract:
The invention relates to tuned multifunctional linker molecules for charge transport through organic-inorganic composite structures. The problem underlying the present invention is to provide multifunctional linker molecules for tuning the conductivity in nanoparticle-linker assemblies which can be used in the formation of electronic networks and circuits and thin films of nanoparticles. The problem is solved according to the invention by providing a multi-functional linker molecule of the general structure CON1-FUNC1-X-FUNC2-CON2 in which X is the central body of the molecule, FUNC1 and FUNC2 independently of each other are molecular groups introducing a dipole moment and/or capable of forming intermolecular and/or intramolecular hydrogen bonding networks, and CON1 and CON2 independently of each other are molecular groups binding to nanostructured units comprising metal and semiconductor materials.
Abstract:
There are described new amino acid amides of the formula (I) ##STR1## in which n, R.sup.1, R.sup.2, R.sup.4, R.sup.5, R.sup.6, R.sup.7, X.sup.1, X .sup.2 and X.sup.3 having the meaning given in the description, and a process for their preparation.The new amino acid amides of the formula (I) are used as pesticides,
Abstract:
A compound of the formulaR.sup.1 --NHC(O)NHSC(S)NR.sup.2 R.sup.3wherein R.sup.1 is phenyl; phenyl substituted with halogen, alkyl, NR.sup.4 R.sup.5 wherein R.sup.4 and R.sup.5 are the same or different and are hydrogen or alkyl; alkoxy, alkylthio, methylenedioxy, COOR.sup.6 wherein R.sup.6 is alkyl; or NHCOOR wherein R.sup.7 is alkyl; R.sup.2 and R.sup.3 are the same or different and are alkyl, cycloalkyl or aralkyl, and R.sup.2 plus R.sup.3 are alkylene, oxydialkylene or thiodialkylene.
Abstract:
Novel 1-hydrocarbyl-3-(thiocarbamoylthio)ureas and 1-hydrocarbyl-3-(carbamoylthio)ureas are prepared by reacting, in liquid phase, an appropriate isocyanate and S-thiocarbamoylhydrosulfamine or S-carbamoylhydrosulfamine, e.g., S-(dimethylthiocarbamoyl)-N-methylhydrosulfamine or S-(dimethylcarbamoyl)hydrosulfamine. All the compounds are useful as rubber-curing agents.
Abstract:
The preparation of thiocarbamyl sulfenamides and particularly the preparation of disubstituted-thiocarbamyl cycloalkylsulfenamides may be improved by utilizing an excess of the dithiocarbamate solution which is reacted with the chlorocycloalkylamine and heating the reaction mixture for a short period of time.
Abstract:
Amines and amine derivatives that improve the buffering range, and/or reduce the chelation and other negative interactions of the buffer and the system to be buffered. The reaction of amines or polyamines with various molecules to form polyamines with differing pKa's will extend the buffering range, derivatives that result in polyamines that have the same pKa yields a greater buffering capacity. Derivatives that result in zwitterionic buffers improve yield by allowing a greater range of stability.
Abstract:
Amines and amine derivatives that improve the buffering range, and/or reduce the chelation and other negative interactions of the buffer and the system to be buffered. The reaction of amines or polyamines with various molecules to form polyamines with differing pKa's will extend the buffering range, derivatives that result in polyamines that have the same pKa yields a greater buffering capacity. Derivatives that result in zwitterionic buffers improve yield by allowing a greater range of stability.
Abstract:
Benzyl derivatives of the formula I ##STR1## where A is CH.sub.2, CHCl, CH-alkyl, CH-alkoxy, CH-alkylthio or N-alkoxy,B is OH, alkylthio, alkoxy or alkylamino,U, V, W are hydrogen, halogen, alkyl or alkoxy,D is ##STR2## where R' is hydrogen or alkyl andR is hydrogen, alkyl, cycloalkyl, haloalkyl, halocycloalkyl, cycloalkylalkyl, alkoxyalkyl, alkylthioalkyl, arylthioalkyl, aryloxyalkyl, aryl, arylalkyl, hetaryl, hetaryl-alkyl, hetaryloxyalkyl or heterocyclyl, and fungicides containing these compounds.