Standard

Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand. / Shekhovtsov, Nikita A.; Vinogradova, Katerina A.; Berezin, Alexei S. и др.

в: Inorganic Chemistry Frontiers, Том 7, № 11, 07.06.2020, стр. 2212-2223.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Shekhovtsov, NA, Vinogradova, KA, Berezin, AS, Sukhikh, TS, Krivopalov, VP, Nikolaenkova, EB & Bushuev, MB 2020, 'Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand', Inorganic Chemistry Frontiers, Том. 7, № 11, стр. 2212-2223. https://doi.org/10.1039/d0qi00254b

APA

Shekhovtsov, N. A., Vinogradova, K. A., Berezin, A. S., Sukhikh, T. S., Krivopalov, V. P., Nikolaenkova, E. B., & Bushuev, M. B. (2020). Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand. Inorganic Chemistry Frontiers, 7(11), 2212-2223. https://doi.org/10.1039/d0qi00254b

Vancouver

Shekhovtsov NA, Vinogradova KA, Berezin AS, Sukhikh TS, Krivopalov VP, Nikolaenkova EB и др. Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand. Inorganic Chemistry Frontiers. 2020 июнь 7;7(11):2212-2223. doi: 10.1039/d0qi00254b

Author

Shekhovtsov, Nikita A. ; Vinogradova, Katerina A. ; Berezin, Alexei S. и др. / Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand. в: Inorganic Chemistry Frontiers. 2020 ; Том 7, № 11. стр. 2212-2223.

BibTeX

@article{1b9018b89ebf43a294a0e506d36002aa,
title = "Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand",
abstract = "Silver(i) complexes with 2-amino-4-phenyl-6-methylpyrimidine (L), [Ag3L2(H2O)0.55(NO3)3]n (1) and [Ag2L2(PPh3)2(NO3)2] (2), have been synthesized and structurally characterized. In the solid state the free ligand L demonstrates dual fluorescence: a high energy band at 375 nm is the emission of the monomer L while a low-energy band at 450 nm can be attributed to the emission of the tautomeric dimer, L2-imino, formed in the excited state double proton transfer (ESDPT) process. In the solid state the complexes demonstrate excitation wavelength dependent photoluminescence originating from three emission mechanisms (hereafter abbreviated as A, B and C for complex 1; A′, B′ and C′ for complex 2). The spectroscopic and computational results reveal that these emission mechanisms can be assigned to metal + nitrate anion to ligand L charge transfer phosphorescence (mechanisms A and A′), excimer 1π-π∗ fluorescence (mechanism B), fluorescence of L2-imino dimeric units formed due to ESDPT (mechanism B′) and ligand-centered 1π-π∗/1n-π∗ fluorescence (mechanisms C and C′). The luminescence of complex 1 at λex = 340 nm shows thermochromic behavior; the emission color dramatically changes from blue-green at 77 K to yellowish green at 175 K and white at 300 K.",
keywords = "DOUBLE-PROTON-TRANSFER, GRAPHENE QUANTUM DOTS, DIPOLAR MOLECULES, FLUORESCENCE, PHOTOLUMINESCENCE, TEMPERATURE, DERIVATIVES, POLYMERS, 2-AMINOPYRIMIDINE, COPPER(I)",
author = "Shekhovtsov, {Nikita A.} and Vinogradova, {Katerina A.} and Berezin, {Alexei S.} and Sukhikh, {Taisiya S.} and Krivopalov, {Viktor P.} and Nikolaenkova, {Elena B.} and Bushuev, {Mark B.}",
year = "2020",
month = jun,
day = "7",
doi = "10.1039/d0qi00254b",
language = "English",
volume = "7",
pages = "2212--2223",
journal = "Inorganic Chemistry Frontiers",
issn = "2052-1545",
publisher = "Royal Society of Chemistry",
number = "11",

}

RIS

TY - JOUR

T1 - Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand

AU - Shekhovtsov, Nikita A.

AU - Vinogradova, Katerina A.

AU - Berezin, Alexei S.

AU - Sukhikh, Taisiya S.

AU - Krivopalov, Viktor P.

AU - Nikolaenkova, Elena B.

AU - Bushuev, Mark B.

PY - 2020/6/7

Y1 - 2020/6/7

N2 - Silver(i) complexes with 2-amino-4-phenyl-6-methylpyrimidine (L), [Ag3L2(H2O)0.55(NO3)3]n (1) and [Ag2L2(PPh3)2(NO3)2] (2), have been synthesized and structurally characterized. In the solid state the free ligand L demonstrates dual fluorescence: a high energy band at 375 nm is the emission of the monomer L while a low-energy band at 450 nm can be attributed to the emission of the tautomeric dimer, L2-imino, formed in the excited state double proton transfer (ESDPT) process. In the solid state the complexes demonstrate excitation wavelength dependent photoluminescence originating from three emission mechanisms (hereafter abbreviated as A, B and C for complex 1; A′, B′ and C′ for complex 2). The spectroscopic and computational results reveal that these emission mechanisms can be assigned to metal + nitrate anion to ligand L charge transfer phosphorescence (mechanisms A and A′), excimer 1π-π∗ fluorescence (mechanism B), fluorescence of L2-imino dimeric units formed due to ESDPT (mechanism B′) and ligand-centered 1π-π∗/1n-π∗ fluorescence (mechanisms C and C′). The luminescence of complex 1 at λex = 340 nm shows thermochromic behavior; the emission color dramatically changes from blue-green at 77 K to yellowish green at 175 K and white at 300 K.

AB - Silver(i) complexes with 2-amino-4-phenyl-6-methylpyrimidine (L), [Ag3L2(H2O)0.55(NO3)3]n (1) and [Ag2L2(PPh3)2(NO3)2] (2), have been synthesized and structurally characterized. In the solid state the free ligand L demonstrates dual fluorescence: a high energy band at 375 nm is the emission of the monomer L while a low-energy band at 450 nm can be attributed to the emission of the tautomeric dimer, L2-imino, formed in the excited state double proton transfer (ESDPT) process. In the solid state the complexes demonstrate excitation wavelength dependent photoluminescence originating from three emission mechanisms (hereafter abbreviated as A, B and C for complex 1; A′, B′ and C′ for complex 2). The spectroscopic and computational results reveal that these emission mechanisms can be assigned to metal + nitrate anion to ligand L charge transfer phosphorescence (mechanisms A and A′), excimer 1π-π∗ fluorescence (mechanism B), fluorescence of L2-imino dimeric units formed due to ESDPT (mechanism B′) and ligand-centered 1π-π∗/1n-π∗ fluorescence (mechanisms C and C′). The luminescence of complex 1 at λex = 340 nm shows thermochromic behavior; the emission color dramatically changes from blue-green at 77 K to yellowish green at 175 K and white at 300 K.

KW - DOUBLE-PROTON-TRANSFER

KW - GRAPHENE QUANTUM DOTS

KW - DIPOLAR MOLECULES

KW - FLUORESCENCE

KW - PHOTOLUMINESCENCE

KW - TEMPERATURE

KW - DERIVATIVES

KW - POLYMERS

KW - 2-AMINOPYRIMIDINE

KW - COPPER(I)

UR - http://www.scopus.com/inward/record.url?scp=85090774757&partnerID=8YFLogxK

U2 - 10.1039/d0qi00254b

DO - 10.1039/d0qi00254b

M3 - Article

AN - SCOPUS:85090774757

VL - 7

SP - 2212

EP - 2223

JO - Inorganic Chemistry Frontiers

JF - Inorganic Chemistry Frontiers

SN - 2052-1545

IS - 11

ER -

ID: 25644411