journal article·2019-01-28

Selective Photocatalytic Oxidation of Benzyl Alcohol to Benzaldehyde or C–C Coupled Products by Visible-Light-Absorbing Quantum Dots

Kevin P. McClelland, Emily A. Weiss

ACS Applied Energy Materials· Volume 2· Issue 1
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Abstract

This Forum Article describes the photocatalytic oxidation of benzyl alcohol by visible-light-absorbing colloidal CdS quantum dots (QDs), with 99% selectivity for benzaldehyde or 91% selectivity for C–C coupled products (primarily hydrobenzoin). The selectivity is tuned through the number of low-valent Cd atoms photodeposited on the surfaces of the QDs in situ; this deposition is enhanced by addition of a Cd2+ salt and suppressed by addition of an electron scavenger, anthroquinone-2-sulfonate, to the reaction mixture. In both cases, the external quantum efficiency (number of oxidative equivalents extracted from the QDs per incident photon) of the system is ∼1%.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Quantum Dots Synthesis And Properties · Radical Photochemical Reactions

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry and Center for Light Energy Activated Redox Processes (LEAP), Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, United States

Funding

Basic Energy Sciences · Division of Graduate Education

References (34)

Show source-provided references
1. 10.1021/ar50081a00110.1021/ar50081a001 ↗
2. 10.1021/jo034982c10.1021/jo034982c ↗
3. 10.1002/anie.20090032210.1002/anie.200900322 ↗
4. 10.1039/b700395c10.1039/b700395c ↗
5. 10.1016/j.jcat.2009.06.01810.1016/j.jcat.2009.06.018 ↗
6. 10.1039/B913880N10.1039/B913880N ↗
7. 10.1039/c1ee01476e10.1039/c1ee01476e ↗
8. 10.1016/j.jphotochem.2013.08.02110.1016/j.jphotochem.2013.08.021 ↗
9. 10.1016/S0040-4039(01)81614-210.1016/S0040-4039(01)81614-2 ↗
10. 10.1002/chem.20100216810.1002/chem.201002168 ↗
11. 10.1021/cs300604k10.1021/cs300604k ↗
12. 10.1021/jp208661n10.1021/jp208661n ↗
13. 10.1021/acsami.5b0412810.1021/acsami.5b04128 ↗
14. 10.1021/jacs.6b0686010.1021/jacs.6b06860 ↗
15. 10.1039/c2ob07053g10.1039/c2ob07053g ↗
16. 10.1021/cs401118x10.1021/cs401118x ↗
17. 10.1021/jacs.6b1322010.1021/jacs.6b13220 ↗
18. 10.1021/jacs.6b1337910.1021/jacs.6b13379 ↗
19. 10.1021/acs.chemmater.7b0110910.1021/acs.chemmater.7b01109 ↗
20. 10.1021/acs.chemmater.6b0310610.1021/acs.chemmater.6b03106 ↗
21. 10.1021/jacs.5b1135310.1021/jacs.5b11353 ↗
22. 10.1021/acs.inorgchem.7b0318210.1021/acs.inorgchem.7b03182 ↗
23. 10.1002/anie.20170024310.1002/anie.201700243 ↗
24. 10.1002/anie.20150277310.1002/anie.201502773 ↗
25. 10.1073/pnas.131675511010.1073/pnas.1316755110 ↗
26. 10.1002/bbpc.1983087060510.1002/bbpc.19830870605 ↗
27. 10.1021/j100151a04110.1021/j100151a041 ↗
28. 10.1039/ft992880105510.1039/ft9928801055 ↗
29. 10.1021/j100190a09010.1021/j100190a090 ↗
30. 10.1023/B:THEC.0000013985.94005.c310.1023/B:THEC.0000013985.94005.c3 ↗
31. 10.1021/nn400826h10.1021/nn400826h ↗
32. 10.1021/jp961380710.1021/jp9613807 ↗
33. 10.1016/B978-1-890661-40-3.50013-210.1016/B978-1-890661-40-3.50013-2 ↗
34. 10.1021/acs.jpclett.6b0189910.1021/acs.jpclett.6b01899 ↗