“…To probe the δ-dependent heat-induced ET behavior of viologen compounds, we summarized all known viologen compounds with definite crystal structures that showed thermochromism or heat-induced color change (Tables and ). − As can be seen in Tables and and Figure S1, the probability to undergo thermochromism or heat-induced color change is higher for viologens with small δ values than for ones with large δ values, although the reported coloration temperatures are different. Heating temperature, undoubtedly, has a great effect on heat-induced ET for viologen compounds.…”
Heat-induced electron transfer (ET) is desirable for
some applications,
such as thermal/photothermal catalysis, thermochromic antifake, and
thermal control of molecular recognition, but needs to be avoided
for photochromic or electrochromic windows and other devices. However,
to date, the key structural factors of heat-induced ET for viologen
compounds are still unclear. This work reveals that the planar structures
of viologen moiety may be an important factor for heat-induced ET
and thermochromism, through the summarization of a structural law
from established thermochromic viologen compounds and the experimental
verification using three known compounds with near-planar viologen
moieties. Hence, this work contributes to enhance the probability
of finding thermochromic viologen compounds with heat-induced electron
transfer process.
“…To probe the δ-dependent heat-induced ET behavior of viologen compounds, we summarized all known viologen compounds with definite crystal structures that showed thermochromism or heat-induced color change (Tables and ). − As can be seen in Tables and and Figure S1, the probability to undergo thermochromism or heat-induced color change is higher for viologens with small δ values than for ones with large δ values, although the reported coloration temperatures are different. Heating temperature, undoubtedly, has a great effect on heat-induced ET for viologen compounds.…”
Heat-induced electron transfer (ET) is desirable for
some applications,
such as thermal/photothermal catalysis, thermochromic antifake, and
thermal control of molecular recognition, but needs to be avoided
for photochromic or electrochromic windows and other devices. However,
to date, the key structural factors of heat-induced ET for viologen
compounds are still unclear. This work reveals that the planar structures
of viologen moiety may be an important factor for heat-induced ET
and thermochromism, through the summarization of a structural law
from established thermochromic viologen compounds and the experimental
verification using three known compounds with near-planar viologen
moieties. Hence, this work contributes to enhance the probability
of finding thermochromic viologen compounds with heat-induced electron
transfer process.
“…More intriguingly, 1 shows some special structural features. First, the organic species utilized as SDAs or/and ligands for the preparation of OHCIs are mainly dominated by pyridyl, triazolyl, and imidazolyl derivatives, − but no bifunctional organic species with pyrazinyl and triazolyl groups are applied for the syntheses of OHCIs. Hence, 1 is the only example of OHCIs incorporating bpt – with bifunctional pyrazinyl and triazolyl groups as SDAs and ligands.…”
Section: Resultsmentioning
confidence: 99%
“…The type of the organic components has a significantly structural directing effect on the frameworks of cadmium iodide components. Generally, protonated organic cations as either ligands or structure-directing agents (SDAs) are particularly preferable for a multiplicity of the anionic species [Cd x I y ] x − y (2 x < y ), as exemplified by simple tetrahedron [CdI 4 ] 2– , − ,, dimers [Cd 2 I 6 ] 2– or [Cd 2 I 7 ] 3– , trimers [Cd 3 I 7 ] − or [Cd 3 I 8 ] 2– , tetramer [Cd 4 I 10 ] 2– , hexamer [Cd 6 I 16 ] 4– , and one-dimensional (1-D) chains ∞ [Cd 2 I 6 ] − ,, or ∞ [Cd 5 I 12 ] 2– , while neutral organic molecules result in the formation of various neutral species [Cd x I 2 x ], such as dimer [Cd 2 I 4 ], hexamer [Cd 6 I 12 ], and 1-D chains ∞ [CdI 2 ], ∞ [Cd 3 I 6 ], and ∞ [Cd 4 I 8 ] . Conversely, OHCIs incorporating the cationic species [Cd x I y ] x − y (2 x > y ) are exceedingly scarce, ,, as a result of synthetic difficulties.…”
The exploration of an excellent triple sensor for monitoring
Cu2+, Fe3+, and Cr2O7
2– ions is of exceeding significance because of their
serious effects
on the human body. Herein, optically active 1H-3,5-bis(pyrazinyl)-1,2,4-triazole
(Hbpt) with triazolyl and pyrazinyl groups was applied for the construction
of a new type of organic hybrid cadmium iodide [Cd6I8(bpt)4(H2O)4]·2H2O (1) incorporating a hitherto-unknown [Cd3I4(H2O)2]2+ trimeric-cationic
unit, which shows an orange light emission at 589 nm with a large
Stokes shift of 246 nm. In virtue of the existence of free bifunctional
azole sites as the receptors, 1 exhibits a highly selective
and sensitive sensing property toward Cu2+, Fe3+, and Cr2O7
2– ions in aqueous
solution with lower detection limits of 0.70∼4.46 ppm, which
offers the sole example of cadmium iodide as an excellent triple sensor
for detecting Cu2+, Fe3+, and Cr2O7
2– ions. Moreover, temperature-dependent
luminescent determinations also reveal that 1 can be
used as the potential luminescent molecular thermometer.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.