Cyclometalated Platinum(II) Complexes Simultaneously Catalyze the Cross-Linking of Polysiloxanes and Function as Luminophores
Source abstract
Abstract
A family of the C,N-cyclometalated species [Pt(ppy)Cl(PPh3)], [Pt(ppy)Cl(CNCy)], [Pt(ppy)(CNCy)(PPh3)](OTf), and [Pt(ppy)(CNCy)2](BF4) (ppy = 2-phenylpyridinato-C2,N; Cy = cyclohexyl) was generated from [Pt(ppy)(μ-Cl)]2, CNCy, and PPh3. The obtained platinum(II) complexes were characterized by high-resolution ESI+-MS, IR, and 1D (1H, 13C{1H}, 195Pt{1H}) and 2D (1H,1H-NOESY; 1H,13C-HSQC; 1H,13C-HMBC) NMR spectroscopy, and the latter three complexes were investigated by X-ray diffraction. All four platinum species were examined as hydrosilylation catalysts (c 10–4–10–3 M; 80–120 °C; [Pt(ppy)Cl(PPh3)] exhibited the highest catalytic activity) for the cross-linking of vinyl-terminated polydimethylsiloxane and polymethylhydrosiloxane to achieve luminescent silicone rubbers. Each solid complex and the appropriate silicone rubber exhibited the same emission spectra in the green region and strong phosphorescence with a solid-state quantum yield of up to 12.5% (measured for the silicone elastomer obtained with the [Pt(ppy)(CNCy)2](BF4) catalyst). The resulting luminescent silicone rubbers can be potentially used for protective coatings (to facilitate the thickness control) and as a component for phosphor-converted white light-emitting diodes (to transform a UV part of the LED emission to the visible spectrum).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Catalytic Cross-Coupling Reactions · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Saint Petersburg State University, Universitetskaya Nab. 7/9, Saint Petersburg, 199034 Russian Federation
South Ural State University, 76, Lenin Av., Chelyabinsk, 454080, Russian Federation
Funding
Russian Science Foundation
References (93)
Show source-provided references
1. Kuah H. X. · 2016 · 13510.1039/9781782623984-00135 ↗
2. 10.1016/j.polymdegradstab.2008.11.01910.1016/j.polymdegradstab.2008.11.019 ↗
3. 10.1007/s40009-013-0150-210.1007/s40009-013-0150-2 ↗
4. 10.1021/cr800199810.1021/cr8001998 ↗
5. 10.1016/j.progpolymsci.2013.11.00310.1016/j.progpolymsci.2013.11.003 ↗
6. 10.1007/s12633-015-9306-710.1007/s12633-015-9306-7 ↗
7. Okura, H.; Wakimoto, T.; Matsui, K.; Matsuda, N.; Suzuki, M.; Kishimoto, T. Wavelength conversion polymer film comprising both inorganic and organic fluorescent compounds, and solar cells employing the wavelength conversion polymer film. WO2014082703A1, 2014.
8. 10.1021/ac00051a01210.1021/ac00051a012 ↗
9. 10.1016/S0956-5663(97)87058-310.1016/S0956-5663(97)87058-3 ↗
10. 10.1039/C8TC01798K10.1039/C8TC01798K ↗
11. 10.1016/S1002-0721(12)60416-510.1016/S1002-0721(12)60416-5 ↗
12. Ziemelis, M. J.; Chang, E.P.; Winnik, M. A. Curable fluorescent organopolysiloxane compositions. EP0719835A1, 1996.
13. 10.1002/app.2974510.1002/app.29745 ↗
14. 10.1117/12.223675310.1117/12.2236753 ↗
15. 10.1016/j.solmat.2012.04.01910.1016/j.solmat.2012.04.019 ↗
16. 10.1039/an993180028910.1039/an9931800289 ↗
17. 10.1016/j.jallcom.2019.07.11610.1016/j.jallcom.2019.07.116 ↗
18. 10.1021/acs.inorgchem.7b0306010.1021/acs.inorgchem.7b03060 ↗
19. 10.1016/j.mee.2013.02.01910.1016/j.mee.2013.02.019 ↗
20. 10.1109/ISPTS.2012.626093410.1109/ISPTS.2012.6260934 ↗
21. 10.1515/nanoph-2018-012610.1515/nanoph-2018-0126 ↗
22. 10.1364/OL.41.00071310.1364/OL.41.000713 ↗
23. 10.1039/C7CY02013A10.1039/C7CY02013A ↗
24. 10.1002/app.2122210.1002/app.21222 ↗
25. 10.1134/S107036321209009510.1134/S1070363212090095 ↗
26. 10.3390/molecules2103031110.3390/molecules21030311 ↗
27. 10.1016/j.jcat.2019.03.00410.1016/j.jcat.2019.03.004 ↗
28. 10.1002/cplu.20150032710.1002/cplu.201500327 ↗
29. 10.1134/S107036321511017110.1134/S1070363215110171 ↗
30. 10.1021/am300502r10.1021/am300502r ↗
31. 10.1016/j.apcata.2009.04.02710.1016/j.apcata.2009.04.027 ↗
32. 10.1134/S003602441509036810.1134/S0036024415090368 ↗
33. 10.1002/chem.20140274610.1002/chem.201402746 ↗
34. 10.1002/app.3467610.1002/app.34676 ↗
35. 10.1002/macp.20110006310.1002/macp.201100063 ↗
36. 10.1007/s11164-017-2875-x10.1007/s11164-017-2875-x ↗
37. 10.1039/C4RA17281G10.1039/C4RA17281G ↗
38. 10.1039/C9RA05948B10.1039/C9RA05948B ↗
39. 10.1021/acscatal.5b0262410.1021/acscatal.5b02624 ↗
40. 10.1021/acs.organomet.8b0046110.1021/acs.organomet.8b00461 ↗
41. 10.1039/C5SC03766B10.1039/C5SC03766B ↗
42. 10.1016/j.ccr.2020.21329810.1016/j.ccr.2020.213298 ↗
43. 10.1021/acsomega.7b0168810.1021/acsomega.7b01688 ↗
44. 10.1016/j.jcat.2013.09.00310.1016/j.jcat.2013.09.003 ↗
45. 10.1071/CH1354610.1071/CH13546 ↗
46. 10.1039/C8CC04287J10.1039/C8CC04287J ↗
47. 10.1021/ic902094c10.1021/ic902094c ↗
48. 10.1002/mrc.127006011210.1002/mrc.1270060112 ↗
49. 10.1134/S107036321510017510.1134/S1070363215100175 ↗
50. 10.1039/cs973020016310.1039/cs9730200163 ↗
51. 10.1002/mrc.249110.1002/mrc.2491 ↗
52. 10.1016/j.jorganchem.2014.02.01610.1016/j.jorganchem.2014.02.016 ↗
53. 10.1016/0022-328X(90)87015-610.1016/0022-328X(90)87015-6 ↗
54. 10.1016/S0277-5387(00)88076-610.1016/S0277-5387(00)88076-6 ↗
55. Kühl O. · 200910.1007/978-3-540-79118-8 ↗
56. Pregosin P. S. · 1979
57. 10.1021/ja963346b10.1021/ja963346b ↗
58. 10.1021/ja065552h10.1021/ja065552h ↗
59. Mason J. · 198710.1007/978-1-4613-1783-8 ↗
60. 10.1021/ic901510m10.1021/ic901510m ↗
61. Iggo J. A. · Modern NMR Techniques for Synthetic Chemistry · 2015 · 177
62. 10.1021/acs.inorgchem.8b0220410.1021/acs.inorgchem.8b02204 ↗
63. 10.1039/C5DT02450A10.1039/C5DT02450A ↗
64. 10.1039/C7NJ04888B10.1039/C7NJ04888B ↗
65. 10.1039/C7NJ03817H10.1039/C7NJ03817H ↗
66. 10.1039/C4RA06623E10.1039/C4RA06623E ↗
67. 10.1021/acs.inorgchem.7b0195610.1021/acs.inorgchem.7b01956 ↗
68. 10.1021/acs.inorgchem.5b0165510.1021/acs.inorgchem.5b01655 ↗
69. Andriot M. · Inorganic Polymers · 2007 · 61
70. Moretto H.-H. · 2000
71. 10.1002/aoc.288110.1002/aoc.2881 ↗
72. 10.1016/j.apcata.2010.03.04110.1016/j.apcata.2010.03.041 ↗
73. 10.1021/acs.organomet.6b0074110.1021/acs.organomet.6b00741 ↗
74. 10.1039/C2DT31339A10.1039/C2DT31339A ↗
75. Marciniec B. · 1992
76. 10.1021/om201036z10.1021/om201036z ↗
77. 10.1021/om800845c10.1021/om800845c ↗
78. 10.1039/D0TC01163K10.1039/D0TC01163K ↗
79. 10.1002/chem.20110188010.1002/chem.201101880 ↗
80. 10.1021/ic501458q10.1021/ic501458q ↗
81. 10.1039/C9SC04239C10.1039/C9SC04239C ↗
82. 10.1021/acs.bioconjchem.0c0054210.1021/acs.bioconjchem.0c00542 ↗
83. 10.1039/C8CS00061A10.1039/C8CS00061A ↗
84. 10.1021/ic00255a02510.1021/ic00255a025 ↗
85. 10.1134/S107036321107023110.1134/S1070363211070231 ↗
86. 10.1002/app.4727210.1002/app.47272 ↗
87. Mok K. L. · Malaysian J. Chem. · 2018 · 20 · 118
88. 10.1021/acs.jchemed.8b0091110.1021/acs.jchemed.8b00911 ↗
89. Handbook G. · 2012
90. Sperling L. H. · 200510.1002/0471757128 ↗
91. Mark J. E. · 200710.1007/978-0-387-69002-5 ↗
92. 10.1016/j.polymdegradstab.2017.05.03010.1016/j.polymdegradstab.2017.05.030 ↗
93. 10.1002/asia.20170030410.1002/asia.201700304 ↗