New insight in boron chemistry: Application in two-photon absorption
Source abstract
Abstract
Abstract Two groups of one-dimensional (1D) boron containing two-photon absorbing fluorophores have been prepared and characterized. One group includes boron atoms incorporated in the conjugated or pseudo conjugated central core and the other contain a boron cluster as an acceptor group at one end of the fluorophores. Two boron containing central cores (with two boron atoms) have been explored: the cyclodiborazane and the pyrazabole moieties. The chosen boron cluster, p-carborane, contains 10 boron atoms. All the prepared fluorophores present high two-photon absorption cross-sections. Some water-soluble as well as lipophylic dyes have been prepared and used in bio-imaging.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nonlinear Optical Materials Studies · Luminescence and Fluorescent Materials · Boron Compounds in Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (40)
Show source-provided references
1. Belfield · J. Phys. Org. Chem. · 2000 · 13 · 83710.1002/1099-1395(200012)13:12<837::AID-POC315>3.0.CO;2-5 ↗
2. Cumpston · Nature · 1999 · 398 · 5110.1038/17989 ↗
3. Guo · Phys. Status Solidi A · 2005 · 202 · R6610.1002/pssa.200510019 ↗
4. Strickler · Adv. Mater. · 1993 · 5 · 47910.1002/adma.19930050617 ↗
5. Wu · SPIE Proc. · 1992 · 1674 · 77610.1117/12.130367 ↗
6. Kawata · Nature · 2001 · 412 · 69710.1038/35089130 ↗
7. Wang · Opt. Lett. · 2002 · 27 · 134810.1364/OL.27.001348 ↗
8. Serbin · Opt. Lett. · 2003 · 28 · 30110.1364/OL.28.000301 ↗
9. Spangler · J. Mater. Chem. · 1999 · 9 · 201310.1039/a902802a ↗
10. Nguyen · Adv. Funct. Mater. · 2005 · 15 · 20910.1002/adfm.200400212 ↗
11. Coenjarts · Chem. Mater. · 2004 · 16 · 555610.1021/cm048717z ↗
12. Anémian · J. Mater. Chem. · 2003 · 13 · 2157216310.1039/B304619B ↗
13. Silly · Chem. Phys. Lett. · 2003 · 379 · 7410.1016/j.cplett.2003.08.017 ↗
14. Helmchen · Nat. Methods · 2005 · 2 · 93210.1038/nmeth818 ↗
15. Cruz · Front. Biosci. · 2005 · 10 · 226310.2741/1696 ↗
16. Molitoris · Am. J. Physiol. · 2005 · 288 · F108410.1152/ajprenal.00473.2004 ↗
17. Karotki · Photochem. Photobiol. · 2006 · 82 · 44310.1562/2005-08-24-RA-657 ↗
18. Belfield · J. Fluo. · 2006 · 16 · 10510.1007/s10895-005-0008-1 ↗
19. Oar · Chem. Mater. · 2005 · 17 · 226710.1021/cm047825i ↗
20. Fournier · Photochem. Photobiol. Sci. · 2004 · 3 · 12010.1039/B302787B ↗
21. Schultz · ACS Chem. Biol. · 2010 · 5 · 44710.1021/cb1001125 ↗
22. Warther · Bioorg. Med. Chem. · 2010 · 18 · 775310.1016/j.bmc.2010.04.084 ↗
23. Warther · J. Am. Chem. Soc. · 2010 · 132 · 258510.1021/ja9074562 ↗
24. Bolze · NLOQO · 2010 · 40 · 253
25. Specht · HFSP J. · 2009 · 3 · 25510.2976/1.3132954 ↗
26. Gug · Angew. Chem. Int. Ed. · 2008 · 47 · 952595-2910.1002/anie.200803964 ↗
27. Hayek · Photochem. Photobiol. Sci. · 2006 · 5 · 10210.1039/B509843B ↗
28. Hayek · Bioconj. Chem. · 2007 · 18 · 84410.1021/bc060362h ↗
29. Bolze · Nonlin. Opt. Quantum Opt. · 2010 · 40 · 253
30. Smith · Cancer Res. · 2001 · 61 · 8179
31. Soloway · Chem. Rev. · 1998 · 98 · 151510.1021/cr941195u ↗
32. Jori · Appl. Radiat. Isot. · 2009 · 67 · S32110.1016/j.apradiso.2009.03.071 ↗
33. Hayek · Angew. Chem. Int. Ed. · 2006 · 45 · 646610.1002/anie.200602266 ↗
34. Hayek · Inorg. Chem. · 2009 · 48 · 911210.1021/ic900627g ↗
35. Matsumoto · Polym. Bull. · 2005 · 53 · 15510.1007/s00289-004-0327-4 ↗
36. Cavero · Angew. Chem. Int. Ed. · 2007 · 46 · 517510.1002/anie.200700820 ↗
37. Matsumi · Polym. J. · 2008 · 40 · 7710.1295/polymj.PJ2007170 ↗
38. Sitha · J. Phys. Chem. A · 2001 · 105 · 872710.1021/jp011134h ↗
39. Hayek · Microsc. Res. Technol. · 2007 · 70 · 88010.1002/jemt.20493 ↗
40. J.-F. Nicoud, F. Bolze, X.H. Sun, A. Hayek, P.L. Baldeck, Inorg. Chem. 2011, accepted for publication.