PbADC and PbADC·H 2 O: Two Coordination Polymers with Acetylenedicarboxylate (ADC 2– ) as Bridging Ligand
Abstract Single crystals of PbADC ( 1 ) and PbADC · H 2 O ( 2 ) formed at the phase boundary of an aqueous silica gel containing acetylenedicarboxylic acid (HOOC–C≡C–COOH, H 2 ADC) and an aqueous solution containing Pb(NO 3 ) 2 . By choosing different concentrations of Pb(NO 3 ) 2 , compounds 1 and...
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Published in | Zeitschrift für anorganische und allgemeine Chemie (1950) Vol. 636; no. 6; pp. 1026 - 1031 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
01.05.2010
|
Online Access | Get full text |
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Summary: | Abstract
Single crystals of PbADC (
1
) and PbADC
·
H
2
O (
2
) formed at the phase boundary of an aqueous silica gel containing acetylenedicarboxylic acid (HOOC–C≡C–COOH, H
2
ADC) and an aqueous solution containing Pb(NO
3
)
2
. By choosing different concentrations of Pb(NO
3
)
2
, compounds
1
and
2
were obtained as phase pure products. Additionally,
1
was obtained by grinding Pb(CH
3
COO)
2
·
3H
2
O with H
2
ADC resulting in a polycrystalline sample. The crystal structures of
1
(
I
4
1
/
amd
,
Z
= 4; SrADC type structure) and
2
(
P
2
1
/
c
,
Z
= 4, new structure type) were solved and refined from X‐ray single crystal data. Compound
1
exhibits a three‐dimensional framework structure: lead cations with a diamond‐like arrangement are interconnected by bridging ADC
2–
ligands. In
2
double‐layers are formed by lead cations, bridging ADC
2–
anions, and water molecules. These layers are held together by hydrogen bonds through water molecules and oxygen atoms of the ADC
2–
ligands. Suspending
1
for 24 h in water at ambient conditions leads to the formation of
2
, which can be converted to
1
again by careful dehydration at approx. 400 K in vacuo. This reversible reaction can be structurally interpreted as a topochemical reaction, which transforms a 3D coordination network into a 2D network structure and vice versa, as both crystal structures show noticeable structural similarities. |
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ISSN: | 0044-2313 1521-3749 |
DOI: | 10.1002/zaac.201000019 |