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Chapter 15 Molecular Luminescence Spectrometry
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A very sensitive and selective instrumental technique with some of the lowest LOD's for molecules that luminesce (not all do!) - down to single-molecule detection. diamagnetic paramagnetic isoelectronic in external magnetic field isoelectronicsplits into 3 energy levels short (ns) lifetimes; "allowed" longer ( s or longer) lifetimes; "forbidden" large small
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Note: fluorescence, phosphorescence, and non-radiative decay can all occur simultaneously depending on the "quantum yields". ps (Jablonski Diagrams)
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The quantum yield for a given process is the ratio of the number of molecules that undergo a particular process to the total number of excited states. SoSo S1S1 T1T1
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Kasha's Rule: fluorescence in fluid solution always occurs from the lowest vibrational level of the 1 st excited singlet state. S o ( ) collisions C = O H H. : ** e-e C O H H : : e-v C = O H H : : ~ ~ solvent molecules S 1 ( *) S o ( ) S 1 ( *) e-t
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SoSo S3S3 S2S2 S1S1 Favored by overlapping vibrational levels. SoSo S1S1 T1T1 Change in spin state from a singlet to a triplet and vica-versa. Heavy atom effect – atoms and small molecules such as Hg, Br 2, I 2, and O 2 have large “spin-orbit coupling” that helps flip spin.
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excited state population C → time → CoCo unique and useful for identification inversely proportional to C o = initial population of the excited state k = 1 st order rate constant (units s -1 )
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Most intense from molecules containing multiple aromatic rings, → * transitions, and structural rigidity. no fluorescence fluorescence f = 1.0 f = 0.2
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excitation spectra – measure luminescence at a fixed wavelength while scanning the excitation wavelengths. emission spectra - excite at a fixed wavelength while scanning the luminescence. excitation spectra – measure luminescence at a fixed wavelength while scanning the excitation wavelengths. emission spectra - excite at a fixed wavelength while scanning the luminescence. overlap at the 0-0 band.
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http://en.wikipedia.org/wiki/Image:Xenon_short_arc_1.jpg
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The absorbance compensating cell contains the dye molecule Rhodamine B which absorbs all wavelengths equally and emits in a pattern that mimics the variation in the lamp output. The corrected excitation spectra are produced by dividing the raw spectrum with the Rhodamine B spectrum.
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The ability to distinguish and identify different molecules based on differences in luminescence spectra. Frequently enhanced by cooling the sample.
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PoPo PtPt PfPf P f = f P a = f (P o – P t ) = f P o (1 – P t /P o ) from Beer’s Law: PtPaPtPa = 10 - bc so P f = f P o (1 – 10 - bc ) Converting to base e and expanding e - bc in a MacLaurin Series* – P f = f P o (1 – 2.303e - bc ) P f = f P o [2.303 bc – (2.303 bc) 2 /2! + (2.303 bc) 3 /3! +….. P f = f P o 2.303 bc *
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A = -log P/P o Why fluorescence is inherently more sensitive.
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anthracene (MW = 178)
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1.Fluorimetric Determination of Inorganic Species 2.Fluorimetric Determination of Organic Species 3.Forensics (latent blood stains - luminol chemiluminescence) 4.Fluorescence Imaging Methods
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Polynuclear Aromatic Hydrocarbons (PAH's) in the environment. perylene 1,2-benzanthracene anthracene fluorescence LOD phosphorescence LOD (parts per trillion) (parts per billion) 3 3 8 0.1 1 ---
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http://en.wikipedia.org/wiki/Luminol
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http://www.microscopyu.com/articles/fluorescence/fluorescenceintro.html
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