Abstract: Disclosed herein are novel light-emitting materials of Formula I and II below. These new complexes are synthesized and found to be sufficiently stable to allow sublimation and vacuum deposition. These new emitters are electrophosphorescent and can be used in organic light-emitting devices (OLEDs) for device elements capable of emitting light of color ranging from orange to red with high-efficiency and high-brightness. wherein E=Group 16 elements (including sulphur); M=Group 10 metal (including platinum); R1-R14 are each independently selected from the group consisting of hydrogen; halogen; alkyl; substituted alkyl; aryl; substituted aryl, with substituents selected from the group consisting of halogen, lower alkyl and recognized donor and acceptor groups. R1 can also be selected from (C?C)nR15, where (C?C) represents a carbon-carbon triple bond (acetylide group), n is selected from 1 to 10, and R15 is selected from alkyl, aryl, substituted aryl, and tri(alkyl)silyl.

Abstract: Disclosed herein are novel light-emitting materials of Formula I and II below. These new complexes are synthesized and found to be sufficiently stable to allow sublimation and vacuum deposition. These new emitters are electrophosphorescent and can be used in organic light-emitting devices (OLEDs) for device elements capable of emitting light of color ranging from orange to red with high-efficiency and high-brightness. wherein E=Group 16 elements (including sulphur); M=Group 10 metal (including platinum); R1-R14 are each independently selected from the group consisting of hydrogen; halogen; alkyl; substituted alkyl; aryl; substituted aryl, with substituents selected from the group consisting of halogen, lower alkyl and recognized donor and acceptor groups. R1 can also be selected from (C?C)nR15, where (C?C) represents a carbon-carbon triple bond (acetylide group), n is selected from 1 to 10, and R15 is selected from alkyl, aryl, substituted aryl, and tri(alkyl)silyl.

Abstract: A catalyst compound of formula I or II: (wherein R1–R11, M, E, T, X, Y, m and n are defined herein). The compound, when combined with a suitable activator, is active for the polymerization of olefins. In an embodiment of combinations of the R1–R7 and T groups, these catalysts can engage in weak attractive non-covalent interactions with the polymer chain. In another embodiment, the R1–R11 groups in formula II exhibit weak attractive non-covalent interactions with the polymer chain.

Abstract: Disclosed herein are novel light-emitting materials of Formula I and II below. These new complexes are synthesized and found to be sufficiently stable to allow sublimation and vacuum deposition. These new emitters are electrophosphorescent and can be used in organic light-emitting devices (OLEDs) for device elements capable of emitting light of color ranging from orange to red with high-efficiency and high-brightness. wherein E=Group 16 elements (including sulphur); M=Group 10 metal (including platinum); R1-R14 are each independently selected from the group consisting of hydrogen; halogen; alkyl; substituted alkyl; aryl; substituted aryl, with substituents selected from the group consisting of halogen, lower alkyl and recognized donor and acceptor groups. R1 can also be selected from (C?C)nR15, where (C?C) represents a carbon-carbon triple bond (acetylide group), n is selected from 1 to 10, and R15 is selected from alkyl, aryl, substituted aryl, and tri(alkyl)silyl.

Abstract: An olefin polymerization catalyst system is prepared from a catalyst of formula I or II: R1–R7 and R1–R12 in formulae I and II, respectively, are each independently —H, -halo, —NO2, —CN, —(C1–C30)hydrocarbyl, —O(C1–C30)hydrocarbyl, —N((C1–C30)hydrocarbyl)2, —Si((C1–C30)hydrocarbyl)3, —(C1–C30)heterohydrocarbyl, -aryl, or -heteroaryl, each being unsubstituted or substituted with one or more —R8 and —R12 groups, respectively. Two R1–R7 can be joined to form a cyclic group. R8 in formula I is -halo, —(C1–C30)hydrocarbyl, —O(C1–C30)hydrocarbyl, —NO2, —CN, —Si((C1–C30)hydrocarbyl)3, —N((C1–C30)hydrocarbyl)2, —(C1–C30)heterohydrocarbyl, -aryl, or -heteroaryl. T in formula I is —CR9R10— wherein R9 and R10 are defined as for R1 above. R12 is independently -halo, —NO2, —CN, —(C1–C30)hydrocarbyl, —O(C1–C30)hydrocarbyl, —N((C1–C30)hydrocarbyl)2, —Si((C1–C30)hydrocarbyl)3, —(C1–C30)heterohydrocarbyl, -aryl, or -heteroaryl. E, M, m, X, Y, and n in formulae I and II are defined herein.

Abstract: A compound of formula I: 1

Abstract: Disclosed herein are compounds shown as Formula I: wherein R1-R11 are each independently selected from a group comprising hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl, and substituted heterohydrocarbyl containing 1 to 20 carbon atoms and two or more of the R1-R11 groups may be joined to form cyclic versions; R1-R11 can also be selected from hydrogen, halogen, and recognized donor and acceptor groups; E is a Group 16 element (including oxygen); M is a metal selected from the group comprising Group 3 to 10 elements (including titanium and zirconium) and the Lanthanide series elements; m is the oxidation state of the metal; X is a monovalent atom or group bonded to M; Y is a mono- or bidentate molecule datively bound to M, and n is zero or an integer up to five. These catalysts, when combined with a suitable activator, are active for the polymerization of olefins.

Abstract: Disclosed herein are compounds shown as Formula I: 1

Abstract: Disclosed herein are novel light-emitting materials of Formula I and II below. These new complexes are synthesized and found to be sufficiently stable to allow sublimation and vacuum deposition. These new emitters are electrophosphorescent and can be used in organic light-emitting devices (OLEDs) for device elements capable of emitting light of color ranging from orange to red with high-efficiency and high-brightness.