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2Im

2Im is an abbreviation encountered in chemical and materials literature that can refer to more than one concept, depending on context. In many cases, 2Im denotes either the 2-substituted imidazole fragment or, more generally, derivatives of imidazole that are substituted at the 2-position. Because there is no universally standardized meaning, the exact interpretation of 2Im should be inferred from the surrounding text, experimental section, or database entry.

Imidazole is a five-membered heteroaromatic ring containing two nitrogen atoms. When a substituent occupies the 2-position,

In practical terms, 2Im frequently appears in discussions of metal-organic frameworks (MOFs) and related coordination polymers,

See also: imidazole, 2-substituted imidazoles, metal-organic frameworks, coordination chemistry.

the
resulting
2-substituted
imidazole
compounds
are
a
common
class
used
as
ligands
in
coordination
chemistry.
Such
ligands
can
bind
to
metal
centers
through
the
nitrogen
atoms
of
the
imidazole
ring,
influencing
coordination
geometry,
electronic
properties,
and
catalytic
activity.
The
2-position
substitution
also
allows
tuning
of
steric
and
solubility
characteristics,
which
can
be
important
in
complex
synthesis
and
material
design.
where
2-substituted
imidazole
derivatives
may
serve
as
linkers
or
modulators.
Derivatives
like
2-methylimidazole
or
other
2-substituted
variants
are
common
examples
used
to
tailor
framework
stability
and
porosity.
Outside
of
coordination
chemistry,
the
term
is
less
standardized;
in
biochemistry,
the
related
imidazole
ring
is
a
component
of
histidine
and
other
biological
molecules,
though
the
shorthand
2Im
is
not
routinely
used
there.