Inventor
MAYER CARL W
CH35 patents
⚠️ This page may combine multiple inventors who share the name “MAYER CARL W”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.
CIBA GEIGY CORP
34 patentsUS5001243AMar 19, 1991
Substituted naphthacene-5, 12-diones
CIBA GEIGY CORP24 citations93
US5177056AJan 5, 1993
Plastics composition containing superconductors
CIBA GEIGY CORP42 citations92
US5009812AApr 23, 1991
Antistatic and electrically conducting polymers and moulding materials
CIBA GEIGY CORP44 citations92
US4617151AOct 14, 1986
2- or 2,3-substituted 5,6,11,12-tetrathiotetracene and 5,6,11,12-tetraselenotetracene
CIBA GEIGY CORP19 citations82
US4384025AMay 17, 1983
Metallically conducting 5,6,11,12-tetrathiotetracene-iodine charge-transfer complex and processes for the production thereof
CIBA GEIGY CORP25 citations82
US4522754AJun 11, 1985
Metallically conducting (2-fluoro-5,6,11,12-tetraselenotetracene)2 -bromide
CIBA GEIGY CORP23 citations78
US5616287AApr 1, 1997
Antistatic and electrically conducting composition
CIBA GEIGY CORP9 citations74
US5324791AJun 28, 1994
Antistatic and electrically conducting composition
CIBA GEIGY CORP4 citations74
US5153321AOct 6, 1992
Antistatic and electrically conducting polymers and moulding materials
CIBA GEIGY CORP13 citations74
US5112977AMay 12, 1992
Substituted naphthacene-5,12-diones
CIBA GEIGY CORP6 citations74
US5011944AApr 30, 1991
Substituted α-pyrones
CIBA GEIGY CORP9 citations74
US4981962AJan 1, 1991
Substituted tetrathiotetracenes and tetraselenotetracenes
CIBA GEIGY CORP7 citations74
US4801701AJan 31, 1989
Difluorinated (5,6,11,12-tetraselenotetracene)2 halides, the preparation thereof and the use thereof
CIBA GEIGY CORP11 citations74
US4601853AJul 22, 1986
(2-fluoro-5,6,11,12-tetraselenotetracene)2 chloride
CIBA GEIGY CORP15 citations74
US4505858AMar 19, 1985
Process for producing 3,4,9,10-tetrathioperylene and 3,4,9,10-tetraselenoperylene
CIBA GEIGY CORP12 citations74
US5504217AApr 2, 1996
Radical cation salts of tetrathiotetracene and copper chloride, their preparation and the use thereof
CIBA GEIGY CORP4 citations73
US5387627AFeb 7, 1995
Radical cation slats of tetrathiotetracene and copper chloride, their preparation and the use thereof
CIBA GEIGY CORP6 citations73
US5284600AFeb 8, 1994
Radical cation salts of tetrathiotetracene and copper chloride, their preparation and the use thereof
CIBA GEIGY CORP9 citations73
US5158829AOct 27, 1992
Electroactive ultra-thin layers
CIBA GEIGY CORP13 citations73
US5108841AApr 28, 1992
Electroactive ultra-thin layers
CIBA GEIGY CORP7 citations73
US5506313AApr 9, 1996
Phosphorus-containing flameproofing agents for epoxy resin materials
CIBA GEIGY CORP8 citations70
US5424372AJun 13, 1995
Antistatic and electrically conducting composition
CIBA GEIGY CORP3 citations63
US5206390AApr 27, 1993
Substituted bisacyloxynaphthacenes
CIBA GEIGY CORP4 citations63
US5200113AApr 6, 1993
Antistatic and electrically conducting composition
CIBA GEIGY CORP1 citations63
US5077156ADec 31, 1991
Antistatic and electrically conductive relief images, processes for the production thereof, coating agents and radiation-sensitive polymers
CIBA GEIGY CORP4 citations63
US4847441AJul 11, 1989
Difluorotetrachlorophenanthrenes
CIBA GEIGY CORP1 citations63
US3984593AOct 5, 1976
5,6,11,12-Tetraselenotetracene-o-chloroanil complexes
CIBA GEIGY CORP2 citations63
US5417911AMay 23, 1995
Process for the preparation of tetraselenotetracene halides and electrically conductive polymer compositions
CIBA GEIGY CORP1 citations52
US5391749AFeb 21, 1995
Substituted naphthacene-5,12-diones and their use
CIBA GEIGY CORP1 citations52
US5338863AAug 16, 1994
Process for the preparation of tetrathiotetracenes
CIBA GEIGY CORP0 citations52
US5220048AJun 15, 1993
Substituted benzocyclobutenes, a process for their preparation and their use
CIBA GEIGY CORP1 citations52
US5096780AMar 17, 1992
Electrically conductive coating comprising a needle network of change transfer complexes
CIBA GEIGY CORP1 citations52
US5084567AJan 28, 1992
Substituted tetrachalcogenofulvalenes and a process for their preparation
CIBA GEIGY CORP1 citations51
US5284942AFeb 8, 1994
Process for the preparation of peri-dichalcogeno polycyclic aromatic compounds
CIBA GEIGY CORP1 citations43