2004
DOI: 10.1016/j.poly.2004.04.022
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Complexation of uranium(VI) with glycerol 1-phosphate

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Cited by 20 publications
(15 citation statements)
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“…1 ) and uranyl-adenosine monophosphate ( Table 2 ). In addition, very similar TRLFS data were obtained in studies investigating the U(VI) complexation by isolated bacterial cell wall compounds ( Table 2 ), such as glycerol-1-phosphate [36] as well as o -phosphoethanolamine (NH 3 CH 2 CH 2 OPO 3 − ) and 1,2-dimyristoyl-sn-glycero-3-phosphate (DMGP) [37] that represent the polar head and the non-polar tail of phospholipids, the major components of cell membranes. Time-resolved analyses revealed a bi-exponential luminescence decay ( Table 3 ) with luminescence lifetimes of around 3 µs (τ 1 ) and 30 µs (τ 2 ) in all samples incubated at pH 2 and pH 3.…”
Section: Resultssupporting
confidence: 66%
“…1 ) and uranyl-adenosine monophosphate ( Table 2 ). In addition, very similar TRLFS data were obtained in studies investigating the U(VI) complexation by isolated bacterial cell wall compounds ( Table 2 ), such as glycerol-1-phosphate [36] as well as o -phosphoethanolamine (NH 3 CH 2 CH 2 OPO 3 − ) and 1,2-dimyristoyl-sn-glycero-3-phosphate (DMGP) [37] that represent the polar head and the non-polar tail of phospholipids, the major components of cell membranes. Time-resolved analyses revealed a bi-exponential luminescence decay ( Table 3 ) with luminescence lifetimes of around 3 µs (τ 1 ) and 30 µs (τ 2 ) in all samples incubated at pH 2 and pH 3.…”
Section: Resultssupporting
confidence: 66%
“…The red-shift of the peak maxima of about 8 nm, caused by the complexing agents phosphocholine, O-phosphoethanolamine, and O-phosphoserine, is comparable to the shift caused by some other phosphonates like glycerol 1-phosphate (phosphoglycerol) [17], O-phospho-L-threonine [33], fructose 6-phosphate [34], and adenosine 5 0 -triphosphate (ATP) [35]. As a consequence, organic uranyl phosphonate complexes are clearly distinguishable from inorganic uranyl phosphates, which show a stronger redshift of about 10 nm [21,22,32] (see Table 1).…”
Section: Phosphonatesmentioning
confidence: 72%
“…However, it is obvious that O-phosphoserine has the strongest complex behavior of the phosphonates investigated in this study. Only the recently studied phosphoglycerol, which also plays an important role both as polar head group and basic unit of phospholipids, seems to be a stronger complexing agent for the uranyl ion (see Table 2) [17].…”
Section: Phosphonatesmentioning
confidence: 99%
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“…2 at 320 nm excitation. The fluorescent spectrum reflects the symmetrical vibration of the U-O bond, similar to other uranyl-containing materials [15][16][17][18][19][20][21][22][23][24]. The observed emission bands correspond to the electronic transition S 10 !…”
mentioning
confidence: 53%