Folic acid treatment of fragile X males: A further study

1988 ◽  
Vol 30 (1-2) ◽  
pp. 393-399 ◽  
Author(s):  
Gene S. Fisch ◽  
Ira L. Cohen ◽  
Anne C. Gross ◽  
Valerie Jenkins ◽  
Edmund C. Jenkins ◽  
...  
Keyword(s):  
1986 ◽  
Vol 23 (1-2) ◽  
pp. 273-289 ◽  
Author(s):  
U. Froster-Iskenius ◽  
K. Bödeker ◽  
T. Oepen ◽  
R. Matthes ◽  
U. Piper ◽  
...  

2008 ◽  
Vol 27 (5) ◽  
pp. 463-467 ◽  
Author(s):  
Karl-Henrik Gustavson ◽  
Kate Dahlbom ◽  
Anders Flood ◽  
Gösta Holmgren ◽  
Hans K→son Blomquist ◽  
...  

1986 ◽  
Vol 23 (1-2) ◽  
pp. 263-271 ◽  
Author(s):  
W. Ted Brown ◽  
Ira L. Cohen ◽  
Gene S. Fisch ◽  
Enid G. Wolf-Schein ◽  
Valerie A. Jenkins ◽  
...  

1986 ◽  
Vol 7 (4) ◽  
pp. 253-256 ◽  
Author(s):  
LYNDA S. MADISON ◽  
THOMAS E. WELLS ◽  
TODD E. FRISTO ◽  
CURTIS G. BENESCH

2010 ◽  
Author(s):  
José-Ramón Rueda ◽  
Javier Ballesteros ◽  
Virginia Guillen ◽  
Maria-Isabel Tejada ◽  
Ivan Solà

2019 ◽  
Author(s):  
Rieko Kobayashi ◽  
Takafumi Ishii ◽  
Yasuo Imashiro ◽  
Jun-ichi Ozaki

Herein, we synthesized N- and P-doped carbons (PN-doped carbons) by controlled phosphoric acid treatment (CPAT) of folic acid (FA) and probed their ability to catalyze the oxygen reduction reaction at the cathode of a fuel cell. Precursors obtained by heating FA in the presence of phosphoric acid at temperatures of 400–1000 °C were further annealed at 1000 °C to afford PN-doped carbons. The extent of precursor P-doping was maximized at 700 °C, and the use of higher temperatures resulted in activation and increased porosity rather than in increased P content. The P/C atomic ratios of PN-doped carbons were well correlated with those of precursors, which indicated that CPAT was well suited for the preparation of PN-doped carbons. Carbon prepared using a CPAT temperature of 700 °C exhibited the highest oxygen reduction reaction (ORR) activity and was shown to contain –C–PO2 and –C–PO3 moieties as the major P species and pyridinic N as the major N species; moreover, no N–P bonds were detected. The presence of –C–PO2 and –C–PO3 units was concluded to decrease the work function and thus raise the Fermi level above the standard O2/H2O reduction potential, which resulted in enhanced ORR activity. Finally, CPAT was concluded to be applicable to the synthesis of PN-doped carbons from N-containing organic compounds other than FA.


1996 ◽  
Vol 13 (3) ◽  
pp. 275-283 ◽  
Author(s):  
Qi Zhao ◽  
Richard R. Behringer ◽  
Benoit de Crombrugghe

Author(s):  
José-Ramón Rueda ◽  
Javier Ballesteros ◽  
Virginia Guillen ◽  
Maria-Isabel Tejada ◽  
Ivan Solà

2019 ◽  
Vol 10 ◽  
pp. 1497-1510 ◽  
Author(s):  
Rieko Kobayashi ◽  
Takafumi Ishii ◽  
Yasuo Imashiro ◽  
Jun-ichi Ozaki

Herein, we synthesized P- and N-doped carbon materials (PN-doped carbon materials) through controlled phosphoric acid treatment (CPAT) of folic acid (FA) and probed their ability to catalyze the oxygen reduction reaction (ORR) at the cathode of a fuel cell. Precursors obtained by heating FA in the presence of phosphoric acid at temperatures of 400–1000 °C were further annealed at 1000 °C to afford PN-doped carbon materials. The extent of precursor P doping was maximized at 700 °C, and the use of higher temperatures resulted in activation and increased porosity rather than in increased P content. The P/C atomic ratios of PN-doped carbon materials correlated well with those of the precursors, which indicated that CPAT is well suited for the preparation of PN-doped carbon materials. The carbon material prepared using a CPAT temperature of 700 °C exhibited the highest ORR activity and was shown to contain –C–PO2 and –C–PO3 moieties as the major P species and pyridinic N as the major N species. Moreover, no N–P bonds were detected. It was concluded that the presence of –C–PO2 and –C–PO3 units decreases the work function and thus raises the Fermi level above the standard O2/H2O reduction potential, which resulted in enhanced ORR activity. Finally, CPAT was concluded to be applicable to the synthesis of PN-doped carbon materials from N-containing organic compounds other than FA.


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