Substitution of the laser borane anti-B18H22 with pyridine: a structural and photophysical study of some unusually structured acropolyhedral boron hydrides
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388980%3A_____%2F18%3A00486863" target="_blank" >RIV/61388980:_____/18:00486863 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1039/c7dt03823b" target="_blank" >http://dx.doi.org/10.1039/c7dt03823b</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c7dt03823b" target="_blank" >10.1039/c7dt03823b</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Substitution of the laser borane anti-B18H22 with pyridine: a structural and photophysical study of some unusually structured acropolyhedral boron hydrides
Popis výsledku v původním jazyce
Reaction of anti-B18H22 1 with pyridine in neutral solvents gives sparingly soluble B16H18-3', 8'-Py-2 3a as the major product (ca. 53%) and B18H20-6', 9'-Py-2 2 (ca. 15%) as the minor product, with small quantities of B18H20-8'-Py 4 (ca. 1%) also being formed. The three new compounds 2, 3a and 4 are characterized by single-crystal X-ray diffraction analyses and by multinuclear multiple-resonance NMR spectroscopy. Compound 2 is of ten-vertex nido: ten-vertex arachno two-atoms-in-common architecture, long postulated for a species with borons-only cluster constitution, but previously elusive. Compound 3a is of unprecedented ten-vertex nido: eight-vertex arachno two-atoms-in-common architecture. The singlecrystal X-ray diffraction analysis for the picoline derivative B16H18(NC5H4Me)(2) 3b, similarly obtained, is also presented. B18H20Py 4 is also previously unreported but is of known ten-vertex nido: ten-vertex nido twoatoms- in-common architecture of anti configuration, but now with the pyridine ligand positioned differently to other reported examples of B18H20L compounds. Factors behind the remarkably low solubility of 3a and 3b are elucidated in terms of electrostatic potential (ESP) calculations, polarity, and van der Waals complementarities. In view of contemporary developing high interest in the fluorescent properties of macropolyhedral boron-containing species, a detailed assessment of the photophysical characteristics of 3a and 4 is also presented. In contrast to the thermochromic fluorescence of 2 (from 620 nm brick-red at room temperature to 585 nm yellow at 8 K, quantum yield 0.15), compound 3a is only weakly phosphorescent in the yellow region (590 nm, quantum yield 0.01), whereas compound 4 exhibits no luminescence. The far more photoactive nature of compound 2 is associated with S-1 excited-state minima structures that differ from each other only by the relative rotational positions of the pyridine substituents on its disubstituted ten-vertex {arachno-B10Py2}-subcluster. The wavelength and relative intensity of fluorescence from these structures depends on the rotational positions of the pyridine ligands, which in turn are influenced by temperature and/or rotational inhibition in the solid-state.
Název v anglickém jazyce
Substitution of the laser borane anti-B18H22 with pyridine: a structural and photophysical study of some unusually structured acropolyhedral boron hydrides
Popis výsledku anglicky
Reaction of anti-B18H22 1 with pyridine in neutral solvents gives sparingly soluble B16H18-3', 8'-Py-2 3a as the major product (ca. 53%) and B18H20-6', 9'-Py-2 2 (ca. 15%) as the minor product, with small quantities of B18H20-8'-Py 4 (ca. 1%) also being formed. The three new compounds 2, 3a and 4 are characterized by single-crystal X-ray diffraction analyses and by multinuclear multiple-resonance NMR spectroscopy. Compound 2 is of ten-vertex nido: ten-vertex arachno two-atoms-in-common architecture, long postulated for a species with borons-only cluster constitution, but previously elusive. Compound 3a is of unprecedented ten-vertex nido: eight-vertex arachno two-atoms-in-common architecture. The singlecrystal X-ray diffraction analysis for the picoline derivative B16H18(NC5H4Me)(2) 3b, similarly obtained, is also presented. B18H20Py 4 is also previously unreported but is of known ten-vertex nido: ten-vertex nido twoatoms- in-common architecture of anti configuration, but now with the pyridine ligand positioned differently to other reported examples of B18H20L compounds. Factors behind the remarkably low solubility of 3a and 3b are elucidated in terms of electrostatic potential (ESP) calculations, polarity, and van der Waals complementarities. In view of contemporary developing high interest in the fluorescent properties of macropolyhedral boron-containing species, a detailed assessment of the photophysical characteristics of 3a and 4 is also presented. In contrast to the thermochromic fluorescence of 2 (from 620 nm brick-red at room temperature to 585 nm yellow at 8 K, quantum yield 0.15), compound 3a is only weakly phosphorescent in the yellow region (590 nm, quantum yield 0.01), whereas compound 4 exhibits no luminescence. The far more photoactive nature of compound 2 is associated with S-1 excited-state minima structures that differ from each other only by the relative rotational positions of the pyridine substituents on its disubstituted ten-vertex {arachno-B10Py2}-subcluster. The wavelength and relative intensity of fluorescence from these structures depends on the rotational positions of the pyridine ligands, which in turn are influenced by temperature and/or rotational inhibition in the solid-state.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10402 - Inorganic and nuclear chemistry
Návaznosti výsledku
Projekt
<a href="/cs/project/GA18-20286S" target="_blank" >GA18-20286S: Klastry hydridů boru pro lasery: Pochopení chemických a strukturálních faktorů, které určují fotofyziku anti-B18H22 a jejích derivátů</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Dalton Transactions
ISSN
1477-9226
e-ISSN
—
Svazek periodika
47
Číslo periodika v rámci svazku
5
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
17
Strana od-do
1709-1725
Kód UT WoS článku
000423760500040
EID výsledku v databázi Scopus
2-s2.0-85041317988