A compound having a Pt tetradentate structure of Formula 1, ##STR00001##
is provided. In the structure of Formula 1, rings C and D each independently represent 5- or 6-membered carbocyclic or heterocyclic ring; L.sup.1, L.sup.2, and L.sup.3 are each independently a direct bond, BR, NR, PR, O, S, Se, C═O, S═O, SO.sub.2, SiRR′, GeRR′, alkyl, cycloalkyl, or a combination thereof; the sum of n1 and n2 is 1 or 2; X is selected from NR.sup.E, O, S, and Se; X.sup.3 and X.sup.4 each independently carbon or nitrogen; and one of Q.sup.1, Q.sup.3, and Q.sup.4 is oxygen, and the remaining two of Q.sup.1, Q.sup.3, and Q.sup.4 each represents a direct bond. Formulations and devices, such as an OLEDs, that include the compound of Formula 1 are also described.

Provided are an organic electroluminescence device, which shows high luminous efficiency, is free of any pixel defect, and has a long lifetime, and a material for an organic electroluminescence device for realizing the device. The material for an organic electroluminescence device is a compound having a π-conjugated heteroacene skeleton crosslinked with a carbon atom, nitrogen atom, oxygen atom, or sulfur atom. The organic electroluminescence device has one or more organic thin film layers including a light emitting layer between a cathode and an anode, and at least one layer of the organic thin film layers contains the material for an organic electroluminescence device.

A metal complex which is useful for production of a light emitting device of which long-term degradation is suppressed is provided. The metal complex is represented by the formula (1):

##STR00001##

wherein, one of Y.sup.a and Y.sup.b is a single bond, and the other is a group represented by the formula (C-1):

##STR00002##

and wherein at least one of Ring R.sup.A, Ring R.sup.B1, Ring R.sup.B2, Ring R.sup.C1 and Ring R.sup.C2 has a group represented by the formula (D-A), the formula (D-B) or the formula (D-C) as a substituent.

A heteroleptic compound having a Formula Ir(L.sub.A).sub.m(L.sub.B).sub.3-m, having a structure of Formula I

##STR00001##

is disclosed. In Formula I, m is 1 or 2; moieties A, C, and D are each independently monocyclic rings or polycyclic fused ring structures; each R.sup.1, R.sup.2, R.sup.A, R.sup.B, R.sup.C, R.sup.D, and R.sup.E is independently hydrogen or a substituent; if moiety A is a monocyclic 6-membered ring, then the R.sup.A para to N of ring A is not an aryl group; at least one of R.sup.1 and R.sup.2 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocycloalkyl, and combinations thereof; and adjacent substituents can be joined to form a ring. OLEDs, consumer products, and formulations including the heteroleptic compound are also disclosed.

A luminescence device includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region. The hole transport region contains a nitrogen-containing compound represented by Formula 1, and thus, the luminescence device may exhibit long lifespan and high efficiency. The substituents are the same as described in the detailed descriptions.

##STR00001##

An organic electroluminescence device includes: a cathode; an anode; and an organic thin-film layer disposed between the cathode and the anode, the organic thin-film layer having one or more layers including an emitting layer, in which the emitting layer includes a first material represented by the following formula (1) and a second material in a form of a fluorescent dopant material. ##STR00001##

Provided herein are processes for preparing fluorescent 1-cyano-2-substituted isoindole compounds or N-substituted phthalazinium compounds, comprising reacting an aromatic dialdehyde or aromatic aldehyde-ketone compound with a material that contains primary amino or hydrazine groups, and assaying methods involving the processes thereof.

A composition which is useful for producing a light emitting device having excellent external quantum efficiency contains two or more compounds represented by the formula (C-1) and a phosphorescent compound, in which at least one of the compounds represented by the formula (C-1) is a compound in which R.sup.C is a group represented by the formula (C′-1). ##STR00001##
Ring R.sup.1C and Ring R.sup.2C represent an aromatic hydrocarbon ring or an aromatic hetero ring. R.sup.C represents an oxygen atom, a sulfur atom or a group represented by the formula (C′-1). ##STR00002##
Ring R.sup.3C and Ring R.sup.4C represent an aromatic hydrocarbon ring or an aromatic hetero ring. R.sup.C′ represents a carbon atom, a silicon atom, a germanium atom, a tin atom or a lead atom.

The present disclosure relates to the field of organic light emitting materials, and in particular, to a fluorescent probe compound for zinc ion, as well as a preparation method and use in zinc ion detection thereof. The fluorescent probe compound of the present disclosure has a name of 2-(7-(2,8-dimethyl quinoline-6-yl)-5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl) phenol, and is synthesized with 2,8-dimethyl tetrahydroquinoline and 2-(2-phenolyl)-1,8-naphthyridine as main raw materials. Fluorescence property tests show that the fluorescent probe compound of the present disclosure has a high selectivity and sensitivity for Zn.sup.2+, a high chemical stability and a good water solubility, which particularly suitable for detecting Zn.sup.2+ in a water environment system. The excitation and emission spectrums of the compound are in a visible region, which could serve as a fluorescent probe applied to the field of zinc ion detection.

A series of thermally stable and highly luminescent cyclometalated tetradentate ligand-containing gold(III) compounds was designed and synthesized. The cyclometalated tetradentate ligand-containing gold(III) compounds can be used as light-emitting material for fabrication of light-emitting devices. The cyclometalated tetradentate ligand-containing gold(III) compounds can be deposited as a layer or a component of a layer using a solution-processing technique or a vacuum deposition process. The cyclometalated tetradentate ligand-containing gold(III) compounds are robust and can provide electroluminescence with high efficiency and brightness. More importantly, the vacuum-deposited OLEDs demonstrate long operational stabilities with half-lifetime of over 29,700 hours at 100 cd m.sup.−2.