journal article·2022

Alkyl selenol reactivity with common solvents and ligands: influences on phase control in nanocrystal synthesis

Eric A. Ho, Antony R. Peng, Janet E. Macdonald

Nanoscale· Volume 14· Issue 1
Publisher page

Abstract

This study develops mechanistic understanding of the factors which control the phase in syntheses of copper selenide nanocrystals by investigating how the chemistry of the dodecylselenol reactant is altered by the ligand and solvent environment. 1H NMR and 77Se NMR were used to study how commonly used solvents (octadecene and dioctylether) and ligands (oleylamine, oleic acid, stearylamine, stearic acid and trioctyl phosphine) change the nature of the dodecylselenol reactant at 25 °C, 155 °C and 220 °C. Unsaturations were prone to selenol additons, carboxylates underwent selenoesterification, amines caused the release of H2Se gas, and the phosphine formed phosphine selenide. Adventitious water caused oxidation to didodecyldiselenide. NMR studies were correlated with the phases that resulted in syntheses of nanocrystalline copper selenides, in which berzalianite, umangite or a metastable hexagonal phase were produced as identified by X-ray diffraction, depending on the ligand and solvent environemnts. Formation of the rare hexagonal Cu2-xSe phase could be assigned to cases that included DD2Se2 as a reactive intermediate, or strong L-type ligation of amines which was dependant on alkyl chain length.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Organoselenium and organotellurium chemistry

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

Affiliations

Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA

Funding

National Science Foundation

References (47)

Show source-provided references
1. Tappan · Chem. Mater. · 2018 · 30 · 570410.1021/acs.chemmater.8b02205 ↗
2. Boles · Nat. Mater. · 2016 · 15 · 36410.1038/nmat4578 ↗
3. Wu · J. Solid State Chem. · 2016 · 238 · 27910.1016/j.jssc.2016.03.048 ↗
4. Riha · J. Am. Chem. Soc. · 2011 · 133 · 138310.1021/ja106254h ↗
5. Hernández-Pagán · Chem. Mater. · 2019 · 31 · 461910.1021/acs.chemmater.9b02019 ↗
6. Mahler · J. Am. Chem. Soc. · 2010 · 132 · 95310.1021/ja9034973 ↗
7. Geisenhoff · Chem. Commun. · 2019 · 55 · 885610.1039/C9CC03326B ↗
8. Frenette · Nat. Commun. · 2017 · 8 · 110.1038/s41467-017-01936-z ↗
9. Hendricks · Science · 2015 · 348 · 122610.1126/science.aaa2951 ↗
10. Evans · J. Am. Chem. Soc. · 2010 · 132 · 1097310.1021/ja103805s ↗
11. Macdonald · Chem. Commun. · 2008 · 377710.1039/b805715j ↗
12. Roffey · Nanoscale · 2016 · 8 · 1106710.1039/C6NR00053C ↗
13. Hollingsworth · Chem. Mater. · 2014 · 26 · 628110.1021/cm503174z ↗
14. Yordanov · Colloid Polym. Sci. · 2008 · 286 · 81310.1007/s00396-008-1840-z ↗
15. Jasieniak · J. Phys. Chem. B · 2005 · 109 · 2066510.1021/jp054289o ↗
16. Bullen · Chem. Mater. · 2010 · 22 · 413510.1021/cm903813r ↗
17. Liu · J. Am. Chem. Soc. · 2012 · 134 · 720710.1021/ja300064t ↗
18. Walker · Chem. Commun. · 2014 · 50 · 833110.1039/C4CC02379J ↗
19. Gariano · J. Am. Chem. Soc. · 2017 · 139 · 958310.1021/jacs.7b03706 ↗
20. Ostwald · Phys. Chem. · 1897 · 22 · 289
21. Washington · J. Am. Chem. Soc. · 2012 · 134 · 1704610.1021/ja302964e ↗
22. Gao · J. Am. Chem. Soc. · 2014 · 136 · 672410.1021/ja5020025 ↗
23. Pennycook · Nano Lett. · 2012 · 12 · 303810.1021/nl3008727 ↗
24. McBride · ACS Nano · 2013 · 7 · 835810.1021/nn403478h ↗
25. Soni · CrystEngComm · 2013 · 15 · 545810.1039/c3ce40267c ↗
26. Huang · J. Am. Chem. Soc. · 2010 · 132 · 1586610.1021/ja105132u ↗
27. Low · Chem. Sci. · 2010 · 1 · 51510.1039/c0sc00212g ↗
28. Berends · Chem. Mater. · 2018 · 30 · 383610.1021/acs.chemmater.8b01143 ↗
29. Dilimon · J. Phys. Chem. C · 2011 · 115 · 1820210.1021/jp203652y ↗
30. Dai · J. Phys. Chem. B · 2006 · 110 · 2295110.1021/jp066181u ↗
31. Dhaene · Nano Lett. · 2019 · 19 · 741110.1021/acs.nanolett.9b03088 ↗
32. Yang · Angew. Chem., Int. Ed. · 2005 · 44 · 671210.1002/anie.200502279 ↗
33. Jiang · Cryst. Growth Des. · 2015 · 15 · 356510.1021/acs.cgd.5b00751 ↗
34. Houck · Chem. Mater. · 2018 · 30 · 835910.1021/acs.chemmater.8b04016 ↗
35. Yang · J. Organomet. Chem. · 2009 · 694 · 101610.1016/j.jorganchem.2008.11.030 ↗
36. Pein · Inorg. Chem. · 2011 · 50 · 19310.1021/ic101651p ↗
37. Bureau · Society · 2005 · 33 · 6130
38. Poleschner · Chem. – Eur. J. · 2021 · 27 · 64910.1002/chem.202003461 ↗
39. Luthra · J. Organomet. Chem. · 1988 · 354 · 5110.1016/0022-328X(88)80638-7 ↗
40. Hancock · Org. Biomol. Chem. · 2015 · 13 · 231010.1039/C4OB02434F ↗
41. Hou · Chem. – Eur. J. · 2013 · 19 · 1584710.1002/chem.201302722 ↗
42. Duddeck · Magn. Reson. Chem. · 1993 · 31 · 73610.1002/mrc.1260310809 ↗
43. Sedgwick · J. Org. Chem. · 1952 · 17 · 32710.1021/jo01136a023 ↗
44. Günther · J. Org. Chem. · 1966 · 31 · 120210.1021/jo01342a052 ↗
45. Čapek · Chem. Mater. · 2009 · 21 · 174310.1021/cm900248b ↗
46. Hu · J. Cryst. Growth · 2006 · 297 · 6110.1016/j.jcrysgro.2006.08.038 ↗
47. Menagen · J. Am. Chem. Soc. · 2009 · 131 · 1740610.1021/ja9077733 ↗