Evidence for Singlet-Oxygen Generation and Biocidal Activity in Photoresponsive Metallic Nitride Fullerene−Polymer Adhesive Films
Source abstract
Abstract
The adhesive properties, as measured by bulk tack analysis, are found to decrease in blends of isomerically pure Sc3N@I(h)-C80 metallic nitride fullerene (MNF) and polystyrene-block-polyisoprene-block-polystyrene (SIS) copolymer pressure-sensitive adhesive under white light irradiation in air. The reduction of tack is attributed to the in situ generation of 1O2 and subsequent photooxidative cross-linking of the adhesive film. Comparisons are drawn to classical fullerenes C60 and C70 for this process. This work represents the first demonstration of 1O2 generating ability in the general class of MNFs (M3N@C80). Additional support is provided for the sensitizing ability of Sc3N@I(h)-C80 through the successful photooxygenation of 2-methyl-2-butene to its allylic hydroperoxides in benzene-d(6) under irradiation at 420 nm, a process that occurs at a rate comparable to that of C(60). Photooxygenation of 2-methyl-2-butene is found to be influenced by the fullerene sensitizer concentration and O2 flow rate. Molar extinction coefficients are reported for Sc3N@I(h)-C80 at 420 and 536 nm. Evaluation of the potential antimicrobial activity of films prepared in this study stemming from the in situ generation of 1O2 led to an observed 1 log kill for select Gram-positive and Gram-negative bacteria.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Fullerene Chemistry and Applications · Polymer Nanocomposite Synthesis and Irradiation · Carbon Nanotubes in Composites
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and Biochemistry, University of Southern Mississippi, Hattiesburg, Mississippi 39406, and Chemistry Division, Naval Research Laboratory, Washington, D.C. 20375
References (48)
Show source-provided references
1. Arbogast J. W. · J. Phys. Chem. · 1991 · 95 · 1110.1021/j100154a006 ↗
2. Foote C. S. · Top. Curr. Chem. · 1994 · 169 · 34710.1007/3-540-57565-0_80 ↗
3. Guldi D. M. · Radiat. Phys. Chem. · 1999 · 56 · 44910.1016/S0969-806X(99)00325-4 ↗
4. Guldi D. M. · Acc. Chem. Res. · 2000 · 33 · 69510.1021/ar990144m ↗
5. Markovic Z. · Biomaterials · 2008 · 29 · 356110.1016/j.biomaterials.2008.05.005 ↗
6. Nakamura E. · Bull. Chem. Soc. Jpn. · 1996 · 69 · 214310.1246/bcsj.69.2143 ↗
7. Orfanopoulos M. · Tetrahedron Lett. · 1995 · 36 · 43510.1016/0040-4039(94)02277-I ↗
8. Kai Y. · Fullerenes, Nanotubes, Carbon Nanostruct. · 2003 · 11 · 7910.1081/FST-120018664 ↗
9. Bensasson R. V. · Free Radical Biol. Med. · 2000 · 29 · 2610.1016/S0891-5849(00)00287-2 ↗
10. Bosi S. · Bioorg. Med. Chem. Lett. · 2000 · 10 · 104310.1016/S0960-894X(00)00159-1 ↗
11. Bosi S. · Eur. J. Med. Chem. · 2003 · 38 · 91310.1016/j.ejmech.2003.09.005 ↗
12. Bosi S. · J. Med. Chem. · 2004 · 47 · 671110.1021/jm0497489 ↗
13. Da Ros T. · Chem. Commun. · 1999 · 663
14. Badireddy A. R. · Environ. Sci. Technol. · 2007 · 41 · 662710.1021/es0708215 ↗
15. Tagmatarchis N. · Org. Lett. · 2000 · 2 · 355110.1021/ol0002121 ↗
16. Tagmatarchis N. · J. Org. Chem. · 2001 · 66 · 802610.1021/jo0104678 ↗
17. Tagmatarchis N. · Chem. Commun. · 2001 · 136610.1039/b103679n ↗
18. Alberti M. N. · Tetrahedron · 2006 · 62 · 1066010.1016/j.tet.2006.07.106 ↗
19. Singleton D. A. · J. Am. Chem. Soc. · 2003 · 125 · 131910.1021/ja027225p ↗
20. Stratakis M. · Tetrahedron · 2000 · 56 · 159510.1016/S0040-4020(99)00950-3 ↗
21. Tokuyama H. · J. Org. Chem. · 1994 · 59 · 113510.1021/jo00084a036 ↗
22. Chen Z. · Neuro-Oncology · 2006 · 8 · 492
23. Fatouros P. P. · Radiology · 2006 · 240 · 75610.1148/radiol.2403051341 ↗
24. Pinzon J. R. · Angew. Chem., Int. Ed. · 2008 · 47 · 417310.1002/anie.200800473 ↗
25. Fang J. S. · Environ. Sci. Technol. · 2007 · 41 · 263610.1021/es062181w ↗
26. Lyon D. Y. · Environ. Sci. Technol. · 2006 · 40 · 436010.1021/es0603655 ↗
27. Lyon D. Y. · Nano Lett. · 2008 · 8 · 153910.1021/nl0726398 ↗
28. Lyon D. Y. · Environ. Toxicol. Chem. · 2005 · 24 · 275710.1897/04-649R.1 ↗
29. Li Q. L. · Water Res. · 2008 · 42 · 459110.1016/j.watres.2008.08.015 ↗
30. Barber R. P. · Org. Electron. · 2006 · 7 · 50810.1016/j.orgel.2006.07.004 ↗
31. Dennler G. · Thin Solid Films · 2006 · 511 · 34910.1016/j.tsf.2005.12.091 ↗
32. Janssen R. A. J. · MRS Bull. · 2005 · 30 · 3310.1557/mrs2005.6 ↗
33. Antipov O. L. · Quantum Electron. · 2002 · 32 · 77610.1070/QE2002v032n09ABEH002290 ↗
34. Elim H. I. · J. Nonlinear Opt. Phys. Mater. · 2003 · 12 · 17510.1142/S0218863503001316 ↗
35. Kamanina N. V. · Synth. Met. · 2003 · 139 · 54710.1016/S0379-6779(03)00358-8 ↗
36. Zeng H. P. · J. Appl. Phys. · 2001 · 89 · 653910.1063/1.1368157 ↗
37. Amao Y. · Microchim.Acta · 2003 · 143 · 110.1007/s00604-003-0037-x ↗
38. Phillips J. P. · Polymer · 2007 · 48 · 677310.1016/j.polymer.2007.08.050 ↗
39. Phillips J. P. · J. Appl. Polym. Sci. · 2008 · 109 · 289510.1002/app.28337 ↗
40. Satas D. · 1999
41. Florian S. · J. Mater. Sci. · 2004 · 39 · 64910.1023/B:JMSC.0000011522.74404.fc ↗
42. Sung I. K. · Polym. J. · 1998 · 30 · 18110.1295/polymj.30.181 ↗
43. Stevenson S. · J. Am. Chem. Soc. · 2006 · 128 · 882910.1021/ja060752e ↗
44. Stevenson S. · J. Am. Chem. Soc. · 2007 · 129 · 1625710.1021/ja077305z ↗
45. Arai H. · Jpn J. Appl. Phys., Part 1 · 2001 · 40 · 662310.1143/JJAP.40.6623 ↗
46. Yanagi K. · Chem. Phys. Lett. · 2007 · 435 · 30610.1016/j.cplett.2006.12.092 ↗
47. Pant R. R. · J. Appl. Polym. Sci. · 2008 · 110 · 308010.1002/app.28670 ↗
48. Wynne J. H. · J. Appl. Polym. Sci. · 2008 · 107 · 208910.1002/app.27246 ↗