Substituted naphthoquinones as novel amino acid sensitive reagents for the detection of latent fingermarks on paper surfaces |
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Authors: | R. Jelly C. Lennard J. Almog |
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Affiliation: | a Nanochemistry Research Institute, Department of Chemistry, Curtin University of Technology, GPO Box U1987, Perth, Western Australia 6845, Australia b National Centre for Forensic Studies, Faculty of Applied Science, University of Canberra, Canberra, ACT 2601, Australia c School of Life and Environmental Sciences, Deakin University, 221 Burwood Hwy, Burwood, Victoria 3125, Australia d Casali Institute of Applied Chemistry, Hebrew University, Jerusalem 91904, Israel |
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Abstract: | In this paper, we present our preliminary studies into naphthoquinones as novel reagents for the detection of latent fingermarks on paper. Latent fingermarks deposited on paper substrates were treated with solutions of selected naphthoquinones in ethyl acetate/HFE-7100, with subsequent heating. The selected compounds were 1,4-dihydroxy-2-naphthoic acid, 1,2-naphthoquinone-4-sulfonate, 2-methoxy-1,4-naphthoquinone and 2-methyl-1,4-naphthoquinone. All of the tested compounds yielded purple-brown visible fingermarks, which also exhibited photoluminescence when illuminated with a high intensity filtered light source at 555 nm and viewed through red goggles. Indirect heat using an oven at 150 °C for 1 h was found to be superior to direct heat with an iron, which while providing faster development lead to increased levels of background colouration. Luminescence spectrophotometry revealed differences in photoluminescence characteristics for fingermarks developed with the different naphthoquinones, with excitation over the range 530-590 nm. Luminescence spectrophotometry of developed lysine, glycine and serine spots on paper was used to confirm that the naphthoquinones were reacting with amino acids in the latent fingermark. |
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Keywords: | Naphthoquinones Latent fingermarks Fingerprints Amino acids Paper surfaces Forensic science |
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