Modification of polymer beads by bis(arylcarbene) insertion provides access to materials with similar bulk properties, but different surface chemical characteristics, compared to the unmodified polymer. A subsequent dyeing process using different diazonium salts generates colored polymers with a variety of surface functional groups. XPS and solid state NMR spectra were used to characterize modified and dyed polymers, which showed that this protocol was both successful and general. BET data showed that the surface area changed significantly after modification, while BJH data showed pore size distribution was unchanged. TG/DSC analysis and Elemental Analysis were also used to characterize modified polymers. This permitted calculation and comp...
Vita.Surface modifications of several reactive preformed polymeric materials, such as poly(methyl me...
This thesis is concerned with the chemical modification of polymer surfaces to confer various functi...
The covalent immobilization of synthetic or natural macromolecular compounds containing amino groups...
Modification of polymer beads by bis(arylcarbene) insertion provides access to materials with simila...
Diarylcarbenes have been shown to be suitable for the surface modification of a diverse range of pol...
This thesis is concerned with the chemical surface modification of several commercial industrial pol...
A detailed investigation of the reactions of diaryldiazo compounds for the surface modification of s...
This thesis is concerned with the synthesis of diazo compounds for the introduction of various funct...
Diploma thesis is focused on modification and characterization of polypropylene (PP) products surfac...
We report here a chemical treatment which permits the direct modification of the surface properties ...
The surfaces of poly(methyl methacrylate) and polyethylene are modified either (i) by a two-step pr...
An attractive methodology based on diazonium chemistry has been developed for the surface modificati...
Photochromic materials are available by a postpolymerization surface modification of diverse polymer...
Homopolymerization of alkylarylcarbenes derived from diazirine monomers that featured benzyl alcohol...
A bis(diaryldiazomethane) substituted with amino groups was synthesized and used for the surface mod...
Vita.Surface modifications of several reactive preformed polymeric materials, such as poly(methyl me...
This thesis is concerned with the chemical modification of polymer surfaces to confer various functi...
The covalent immobilization of synthetic or natural macromolecular compounds containing amino groups...
Modification of polymer beads by bis(arylcarbene) insertion provides access to materials with simila...
Diarylcarbenes have been shown to be suitable for the surface modification of a diverse range of pol...
This thesis is concerned with the chemical surface modification of several commercial industrial pol...
A detailed investigation of the reactions of diaryldiazo compounds for the surface modification of s...
This thesis is concerned with the synthesis of diazo compounds for the introduction of various funct...
Diploma thesis is focused on modification and characterization of polypropylene (PP) products surfac...
We report here a chemical treatment which permits the direct modification of the surface properties ...
The surfaces of poly(methyl methacrylate) and polyethylene are modified either (i) by a two-step pr...
An attractive methodology based on diazonium chemistry has been developed for the surface modificati...
Photochromic materials are available by a postpolymerization surface modification of diverse polymer...
Homopolymerization of alkylarylcarbenes derived from diazirine monomers that featured benzyl alcohol...
A bis(diaryldiazomethane) substituted with amino groups was synthesized and used for the surface mod...
Vita.Surface modifications of several reactive preformed polymeric materials, such as poly(methyl me...
This thesis is concerned with the chemical modification of polymer surfaces to confer various functi...
The covalent immobilization of synthetic or natural macromolecular compounds containing amino groups...