2003
DOI: 10.1016/s0925-4005(03)00119-9
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Solid-state optical detection of amino acids

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Cited by 40 publications
(21 citation statements)
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“…PMO-A specific surface area = 157 m 2 /g; PMO-B specific surface area = 144 m 2 /g. on previously published work (Awawdeh et al, 2003;Kibbey and Meyerhoff, 1993;White and Harmon, 2004). Reflectance and fluorescence experiments indicate a lower concentration of porphyrin per square meter in the imprinted PMO (PMO-B) as compared to the non-imprinted PMO (PMO-A).…”
Section: Discussionsupporting
confidence: 59%
See 1 more Smart Citation
“…PMO-A specific surface area = 157 m 2 /g; PMO-B specific surface area = 144 m 2 /g. on previously published work (Awawdeh et al, 2003;Kibbey and Meyerhoff, 1993;White and Harmon, 2004). Reflectance and fluorescence experiments indicate a lower concentration of porphyrin per square meter in the imprinted PMO (PMO-B) as compared to the non-imprinted PMO (PMO-A).…”
Section: Discussionsupporting
confidence: 59%
“…The bands comprising the emission spectrum are more distinctly separated and the ratio of their intensities is different from that of the porphyrin in solution. The change in porphyrin spectrophotometric characteristics upon immobilization has been well documented (Awawdeh et al, 2003;Kibbey and Meyerhoff, 1993;White and Harmon, 2004). The difference spectra presented in Fig.…”
Section: Pmo Detection Of Nitro-energetics and Related Compoundsmentioning
confidence: 75%
“…Amino acids are the building blocks of proteins that are considered to be very important for most of the processes in living organisms [10]. The presence of acidic carboxyl and basic amino group paves the way for the formation of zwitter ion or dipolar ion as a result of internal neutralization reaction.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5][6][7][8][9][10] In the metallation of porphyrins, depending on size, charge, and spin multiplicity of metal ions, they can fit into the center of the porphyrin ring, forming regular metalloporphyrins, or several of them are located out of the ligand plane, resulting in sitting-atop (SAT) complexes. 11 For the first time, these complexes were indicated as intermediate in the metallation processes of the protoporphyrin dimethyl ester in chloroform, in which two pyrrolenine nitrogens coordinate to the metal ion and two protons on the pyrrole nitrogens remain.…”
Section: Introductionmentioning
confidence: 99%