- 9,10-diphenylanthracene (DPA) emits blue light
- 1-chloro-9,10-diphenylanthracene (1-chloro(DPA)) and 2-chloro-9,10-diphenylanthracene (2-chloro(DPA)) emit blue-green light more efficiently than nonsubstituted DPA; dihydro(DPA) is purple
- 9,10-bis(phenylethynyl)anthracene (BPEA) emits yellow-green light with maximum at 486 nm
- 1-chloro-9,10-bis(phenylethynyl)anthracene emits yellow-green light, used in 30-minute high-intensity Cyalume sticks
- 2-chloro-9,10-bis(phenylethynyl)anthracene emits green light, used in 12-hour low-intensity Cyalume sticks
- 1,8-dichloro-9,10-bis(phenylethynyl)anthracene emits yellow light, used in Cyalume sticks
- Rubrene emits orange-yellow at 550 nm
- 2,4-di-tert-butylphenyl 1,4,5,8-tetracarboxynaphthalene diamide emits deep red light, together with DPA is used to produce white or hot-pink light, depending on their ratio
- Rhodamine B emits red light. It is rarely used, as it breaks down in contact with phenyl oxalate, shortening the shelf life of the mixture.
- 5,12-bis(phenylethynyl)naphthacene emits orange light
- Violanthrone emits orange light at 630 nm
- 16,17-(1,2-ethylenedioxy)violanthrone emits red at 680 nm
- 16,17-dihexyloxyviolanthrone emits infrared at 725 nm
- 16,17-butyloxyviolanthrone emits infrared
- N,N'-bis(2,5,-di-tert-butylphenyl)-3,4,9,10-perylenedicarboximide emits infrared
- 1-N,N-dibutylaminoanthracene emits infrared
- 6-methylacridinium iodide emits infrared
9,10-diphenylanthracene yields blue light
9,10-bis(phenylethynyl) anthracene yields green light
1-chloro- 9,10-bis(phenylethynyl) anthracene yields yellow-green light
rubrene (5,6,11,12-tetraphenyl naphthacene) yields yellow light
5,12-bis(phenylethynyl) naphthacene yields orange light
Rhodamine 6G yields orange light
Rhodamine B yields red light
Other articles related to "fluorophores, fluorophore":
... Non-protein organic fluorophores belong to following major chemical families - Xanthene derivatives fluorescein, rhodamine, Oregon green, eosin, and Texas red - Cyanine derivatives cyanine, indocarbocyanine ... violet, malachite green - Tetrapyrrole derivatives porphin, phtalocyanine, bilirubin These fluorophores fluoresce thanks to delocalized electrons which can jump a band and stabilize the energy absorbed ... This discrimates Fluorophores from quantum dots, which are fluorescent semiconductor nanoparticles ...
... A fluorophore (or fluorochrome, similarly to a chromophore) is a fluorescent chemical compound that can re-emit light upon light excitation ... Fluorophores typically contain several combined aromatic groups, or plane or cyclic molecules with several π bonds ... Fluorophores are sometimes used alone, as a tracer in fluids, as a dye for staining of certain structures, as a substrate of enzymes, or as a probe or indicator (when its ...
... This occurs several times, to ensure that all accessible fluorophores are bleached since unbleached fluorophores are exchanged for bleached fluorophores, causing movement ...
... energy from an excited (donor) chromophore or fluorophore (if the chromophores are fluorescent) to a nearby acceptor ... In this method, fluorophores are chemically linked or genetically fused to two proteins hypothesised to interact ... If the proteins interact, this will bring the fluorophores into close spatial proximity ...
... Commonly fluorophores (such as rhodamine or fluorescein) are linked to the ring linked to the sugar (in para) via a flexible arm, presumably extruding from the major groove of the helix ... sequence is typically copied using a nucleotide with an arm and later coupled with a reactive fluorophore (indirect labelling) amine reactive Aminoallyl nucleotide contain a primary amine group on a linker that ... thiol reactive thiol containing nucleotides reacts with the fluorophore linked to a reactive leaving group, such as a maleimide ...