journal article·2021-02-12

Cyclometalated Platinum(II) Complexes Simultaneously Catalyze the Cross-Linking of Polysiloxanes and Function as Luminophores

Mikhail V. Dobrynin, Elina V. Sokolova, Mikhail A. Kinzhalov, Andrey S. Smirnov, Galina L. Starova, Vadim Yu. Kukushkin, Regina M. Islamova

ACS Applied Polymer Materials· Volume 3· Issue 2
Publisher page

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).
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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 ↗