two structural features are critical for the design of colorimetric or fluorometric sensors: functional sites for interaction with analytes, and a chromophore or fluorophore for pairing with the active site. the primary factor is that having numerous classes of strong chemical interactions can be very beneficial, in preference to the van der Waals or physical absorption. based on the kinds of intermolecular interactions which could result in significant colorimetric or fluorometric changes, one can be divided cross-reactive, chemoresponsive dyes into five classes (albeit with a few overlap): (i) acidic dyes or Brønsted base (e. g. , diverse pH markers), (ii) Lewis acid/base dyes (e. g. , metal complexes with open coordination sites or chromogens containing metal ions), (iii) redox dyes, (iv) Dyes with large permanent dipoles (e. g. , zwitterionic vapochromic or solvatochromic dyes) to detect local polarity or hydrogen bonding; further, the preservative matrix of these dyes may be involved in improving their chemical selectivity, both by using modifying the local dye environment or through immobilizing the dye molecules in a sterically confining surroundings (e. g. , molecularly imprinted polymers). Early versions of the colorimetric sensor arrays were made of porphyrins and metalloporphyrins, which were made as sensor components, and mainly used Lewis interactions with metal and Brønsted interactions with free base porphyrins. With the addition of a much wider range of chemical dyes, the variety of sensors has elevated dramatically during the last decade [79]. for example, a lately developed 40-element sensor array that includes an extensive range of chemical dyes has shown promising applications in detecting toxic or explosive vapors [208].
two
structural features are critical for the design of colorimetric or
fluorometric
sensors: functional sites for
interaction
with analytes, and a
chromophore
or
fluorophore
for pairing with the active site.
the
primary factor is that having numerous classes of strong
chemical
interactions
can be
very
beneficial, in preference to the van
der
Waals
or physical absorption.
based
on the kinds of intermolecular
interactions
which could result in significant colorimetric or
fluorometric
changes
, one can
be divided
cross-reactive,
chemoresponsive
dyes
into five classes (albeit with a few overlap): (i) acidic
dyes
or
Brønsted
base (
e. g.
,
diverse pH markers), (ii) Lewis acid/base
dyes
(
e. g.
,
metal complexes with open coordination sites or
chromogens
containing metal ions), (iii) redox
dyes
, (iv)
Dyes
with large permanent dipoles (
e. g.
,
zwitterionic
vapochromic
or
solvatochromic
dyes)
to detect local polarity or hydrogen bonding;
further
, the preservative matrix of these
dyes
may
be involved
in improving their
chemical
selectivity, both by using modifying the local
dye
environment or through immobilizing the
dye
molecules in a
sterically
confining surroundings (
e. g.
,
molecularly
imprinted polymers). Early versions of the colorimetric sensor arrays
were made
of porphyrins and
metalloporphyrins
, which
were made
as sensor components, and
mainly
used
Lewis
interactions
with metal and
Brønsted
interactions
with free base porphyrins. With the addition of a much wider range of
chemical
dyes
, the variety of sensors has elevated
dramatically
during the last decade [79].
for
example, a lately developed 40-element sensor array that includes an extensive range of
chemical
dyes
has shown promising applications in detecting toxic or explosive vapors [208].