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"Two-in-one" organic-inorganic hybrid MnII complexes exhibiting dual-emissive phosphorescence. / Berezin, Alexey S.; Samsonenko, Denis G.; Brel, Valery K. и др.

в: Dalton Transactions, Том 47, № 21, 29.05.2018, стр. 7306-7315.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Berezin, AS, Samsonenko, DG, Brel, VK & Artem'Ev, AV 2018, '"Two-in-one" organic-inorganic hybrid MnII complexes exhibiting dual-emissive phosphorescence', Dalton Transactions, Том. 47, № 21, стр. 7306-7315. https://doi.org/10.1039/c8dt01041b

APA

Vancouver

Berezin AS, Samsonenko DG, Brel VK, Artem'Ev AV. "Two-in-one" organic-inorganic hybrid MnII complexes exhibiting dual-emissive phosphorescence. Dalton Transactions. 2018 май 29;47(21):7306-7315. doi: 10.1039/c8dt01041b

Author

Berezin, Alexey S. ; Samsonenko, Denis G. ; Brel, Valery K. и др. / "Two-in-one" organic-inorganic hybrid MnII complexes exhibiting dual-emissive phosphorescence. в: Dalton Transactions. 2018 ; Том 47, № 21. стр. 7306-7315.

BibTeX

@article{8f6080c35e5d4d6e86d712ffd107b190,
title = "{"}Two-in-one{"} organic-inorganic hybrid MnII complexes exhibiting dual-emissive phosphorescence",
abstract = "Unprecedented organic-inorganic hybrid complexes, [Mn(L)3]MnHal4, containing both four- and hexacoordinated Mn2+ ions were synthesized by reacting MnCl2 or MnBr2 with bis(phosphine oxide) ligands (L) such as dppmO2, dppeO2, and 2,3-bis(diphenylphosphinyl)-1,3-butadiene (dppbO2). In the [Mn(L)3]2+ cation of the complexes, the Mn2+ ion features a [MnO6] octahedral coordination environment (Oh), and the [MnHal4]2- anion adopts a tetrahedral geometry (Td). These {"}two-in-one{"} complexes exhibit strong long-lived luminescence (τav = 12-15 ms at 300 K) having interesting thermochromic behavior attributed to the thermal equilibrium between two emission bands. So, in an emission spectrum of the typical complex [Mn(dppbO2)3]MnBr4, the intense {"}red{"} (ca. 620 nm) and weak {"}green{"} (ca. 520 nm) bands, originating from Mn2+ ions in Oh and Td environments, respectively, are observed. Cooling from 300 to 77 K simultaneously leads to (i) redshift of both bands by ca. 20 nm, (ii) increasing their intensities, and (iii) causing a substantial change of their integral intensity ratio from about 4:1 to 2:1. As a result, the colour of the emission changes from orange (CIE 0.56, 0.45) at 300 K to deep red (CIE 0.62, 0.39) at 77 K. This behavior was rationalized using steady-state and time-resolved fluorescent spectroscopy at various temperatures. The high photoluminescence quantum yields (up to 61% at 300 K) and fascinating dual-emissive phosphorescence coupled with high thermal stability and solubility suggest a high potential of this novel class of emissive Mn2+ complexes as promising emitters for OLED devices and potential stimuli-responsive materials.",
keywords = "TRANSITION-METAL-COMPLEXES, UP-CONVERSION LUMINESCENCE, RED-LIGHT EMISSION, MANGANESE(II) COMPOUNDS, FLUORESCENT PROPERTIES, TETRAHEDRAL COMPLEXES, QUANTUM YIELD, PHOTOLUMINESCENCE, TRIBOLUMINESCENCE, TEMPERATURE",
author = "Berezin, {Alexey S.} and Samsonenko, {Denis G.} and Brel, {Valery K.} and Artem'Ev, {Alexander V.}",
year = "2018",
month = may,
day = "29",
doi = "10.1039/c8dt01041b",
language = "English",
volume = "47",
pages = "7306--7315",
journal = "Dalton Transactions",
issn = "1477-9226",
publisher = "Royal Society of Chemistry",
number = "21",

}

RIS

TY - JOUR

T1 - "Two-in-one" organic-inorganic hybrid MnII complexes exhibiting dual-emissive phosphorescence

AU - Berezin, Alexey S.

AU - Samsonenko, Denis G.

AU - Brel, Valery K.

AU - Artem'Ev, Alexander V.

PY - 2018/5/29

Y1 - 2018/5/29

N2 - Unprecedented organic-inorganic hybrid complexes, [Mn(L)3]MnHal4, containing both four- and hexacoordinated Mn2+ ions were synthesized by reacting MnCl2 or MnBr2 with bis(phosphine oxide) ligands (L) such as dppmO2, dppeO2, and 2,3-bis(diphenylphosphinyl)-1,3-butadiene (dppbO2). In the [Mn(L)3]2+ cation of the complexes, the Mn2+ ion features a [MnO6] octahedral coordination environment (Oh), and the [MnHal4]2- anion adopts a tetrahedral geometry (Td). These "two-in-one" complexes exhibit strong long-lived luminescence (τav = 12-15 ms at 300 K) having interesting thermochromic behavior attributed to the thermal equilibrium between two emission bands. So, in an emission spectrum of the typical complex [Mn(dppbO2)3]MnBr4, the intense "red" (ca. 620 nm) and weak "green" (ca. 520 nm) bands, originating from Mn2+ ions in Oh and Td environments, respectively, are observed. Cooling from 300 to 77 K simultaneously leads to (i) redshift of both bands by ca. 20 nm, (ii) increasing their intensities, and (iii) causing a substantial change of their integral intensity ratio from about 4:1 to 2:1. As a result, the colour of the emission changes from orange (CIE 0.56, 0.45) at 300 K to deep red (CIE 0.62, 0.39) at 77 K. This behavior was rationalized using steady-state and time-resolved fluorescent spectroscopy at various temperatures. The high photoluminescence quantum yields (up to 61% at 300 K) and fascinating dual-emissive phosphorescence coupled with high thermal stability and solubility suggest a high potential of this novel class of emissive Mn2+ complexes as promising emitters for OLED devices and potential stimuli-responsive materials.

AB - Unprecedented organic-inorganic hybrid complexes, [Mn(L)3]MnHal4, containing both four- and hexacoordinated Mn2+ ions were synthesized by reacting MnCl2 or MnBr2 with bis(phosphine oxide) ligands (L) such as dppmO2, dppeO2, and 2,3-bis(diphenylphosphinyl)-1,3-butadiene (dppbO2). In the [Mn(L)3]2+ cation of the complexes, the Mn2+ ion features a [MnO6] octahedral coordination environment (Oh), and the [MnHal4]2- anion adopts a tetrahedral geometry (Td). These "two-in-one" complexes exhibit strong long-lived luminescence (τav = 12-15 ms at 300 K) having interesting thermochromic behavior attributed to the thermal equilibrium between two emission bands. So, in an emission spectrum of the typical complex [Mn(dppbO2)3]MnBr4, the intense "red" (ca. 620 nm) and weak "green" (ca. 520 nm) bands, originating from Mn2+ ions in Oh and Td environments, respectively, are observed. Cooling from 300 to 77 K simultaneously leads to (i) redshift of both bands by ca. 20 nm, (ii) increasing their intensities, and (iii) causing a substantial change of their integral intensity ratio from about 4:1 to 2:1. As a result, the colour of the emission changes from orange (CIE 0.56, 0.45) at 300 K to deep red (CIE 0.62, 0.39) at 77 K. This behavior was rationalized using steady-state and time-resolved fluorescent spectroscopy at various temperatures. The high photoluminescence quantum yields (up to 61% at 300 K) and fascinating dual-emissive phosphorescence coupled with high thermal stability and solubility suggest a high potential of this novel class of emissive Mn2+ complexes as promising emitters for OLED devices and potential stimuli-responsive materials.

KW - TRANSITION-METAL-COMPLEXES

KW - UP-CONVERSION LUMINESCENCE

KW - RED-LIGHT EMISSION

KW - MANGANESE(II) COMPOUNDS

KW - FLUORESCENT PROPERTIES

KW - TETRAHEDRAL COMPLEXES

KW - QUANTUM YIELD

KW - PHOTOLUMINESCENCE

KW - TRIBOLUMINESCENCE

KW - TEMPERATURE

UR - http://www.scopus.com/inward/record.url?scp=85047747313&partnerID=8YFLogxK

U2 - 10.1039/c8dt01041b

DO - 10.1039/c8dt01041b

M3 - Article

C2 - 29770407

AN - SCOPUS:85047747313

VL - 47

SP - 7306

EP - 7315

JO - Dalton Transactions

JF - Dalton Transactions

SN - 1477-9226

IS - 21

ER -

ID: 13668266