Forensic
Analysis
of
Blood using Luminol
|
Luminol
- Redox reaction with oxygen in the presence of catalyst
produces a
bright blue glow.
- Used in forensic analysis for detection of blood
- Iron in hemoglobin acts as catalyst
- Other common catalysts
- Biological: copper and cyanide
- Laboratory: potassium ferricyanide
Chemiluminescence
- Chemical reaction produces an excited state compound
- Excited state compound passes through intermediate
- Decays to ground state
- Emits a photon characteristic to compound
|

Sample of Lumniol
source:
http://en.wikipedia.org/wiki/File:Luminol2006.jpg
|
Chemical
Reactions
1.) Luminol must be activated by hydroxide salt forming a dianion:
In the presence of iron (catalyst), hydrogen peroxide decomposes to
form oxygen
The dianion reacts with oxygen producing the unstable organic peroxide
intermediate:
This intermediate decomposes from higher energy states to the ground
state, emitting a photon.
intersystem crossing is radiationless transition between different
states of spin multiplicity
Chemiluminescense

Chemiluminescense Energy Diagram. As shown by the red dot,
Luminol is excited into the triplet dianion
state chemically. Through intersystem crossing, the
molecule is able to transtion into the singlet dianion state of
the same energy. Finally, the molecule fluoresces from the
singlet dianion state to the ground state dianion
emitting a photon of energy
h
v.
Advantages
- Fluoresces in the presence of other compounds, including bleach
&
horseradish
- Can prevent other testing
- Possible carcinogen
Application

Luminol can be used in a healthcare setting for contamination
assessment (Bergervoet, et. al. 2008).
References
P.W.M.
Bergervoet,
N. van Riessen,
F.W. Sebens,
W.C. van der
Zwet. "Application
of the forensic Luminol for blood in infection control." J
of Hospital Infection. 68 (2008):
329-333.
http://www.3dchem.com/molecules.asp?ID=334
http://www.experiencefestival.com/a/Luminol_-_Use_by_Crime_Scene_Investigators/id/1732139