1986
DOI: 10.1107/s0108270186092387
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Dimeric lithium o-phenylenedioxydiacetate trihydrate

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Cited by 12 publications
(8 citation statements)
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“…The polymer net is stabilized via two medium strength intramolecular hydrogen bonds [23] (Table IV) molecule are comparable to those found for the free acid [24] and its complexes [25][26][27], but standard deviations are considerably smaller. The side-chain conformation, best illustrated by the torsion angle about the oxygen atom from the phenoxy group and an adjacent acetate carbon atom (þ85.8 (3) ), is comparable to that found for the manganese complex (À80.1 ) [25], and quite different from that of the free MCPA molecule (þ173.5 ) [24]. The least-squares planes calculated through the acetate [maximum deviation À0.014(2) Å for C (9)] and the 4-chloro-2-methylphenoxy [maximum deviation À0.052(2) Å for O (1)] groups makes a dihedral angle 84.0(1) .…”
Section: Cadmium(ii) Coordination Polymer 1093mentioning
confidence: 62%
“…The polymer net is stabilized via two medium strength intramolecular hydrogen bonds [23] (Table IV) molecule are comparable to those found for the free acid [24] and its complexes [25][26][27], but standard deviations are considerably smaller. The side-chain conformation, best illustrated by the torsion angle about the oxygen atom from the phenoxy group and an adjacent acetate carbon atom (þ85.8 (3) ), is comparable to that found for the manganese complex (À80.1 ) [25], and quite different from that of the free MCPA molecule (þ173.5 ) [24]. The least-squares planes calculated through the acetate [maximum deviation À0.014(2) Å for C (9)] and the 4-chloro-2-methylphenoxy [maximum deviation À0.052(2) Å for O (1)] groups makes a dihedral angle 84.0(1) .…”
Section: Cadmium(ii) Coordination Polymer 1093mentioning
confidence: 62%
“…Data collection: CrysAlis PRO (Agilent, 2012); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SIR92 (Altomare et al, 1993); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008) within WinGX (Farrugia, 1999); molecular graphics: PLATON (Spek, 2009) (Kennard et al, 1986); (L = 4-chloro-2-methylphenoxyacetate) (Smith et al, 1981); [MgL(H 2 O) 5 ] (L = 2,4,5-trichlorophenoxyacetate) (Smith et al, 1982)], or polymeric [[MgL 2 (H 2 O) 2 ] n (L = phenoxyacetate or 4-chlorophenoxyacetate) (Smith et al, 1980)]. (Table 2), with carboxyl and phenoxy O-atom acceptors as well as with the partial water molecules of solvation (S.O.F.…”
Section: Methodsmentioning
confidence: 99%
“…For the structures of some magnesium complexes, derived from phenoxyacetic acids, see: Smith et al (1980Smith et al ( , 1981Smith et al ( , 1982; Kennard et al (1986). For the structures of other metal complexes with 4-fluorophenoxyacetate, see: O'Reilly et al (1984); Smith et al (1993).…”
Section: Related Literaturementioning
confidence: 99%
“…Of interest have also been the structures of the metal complexes with these acids, including those with magnesium in which the monoanionic phenoxyacetate ligands (L) display a variety of coordination modes, all based on an octahedral MgO 6 metal stereochemistry. These include discrete monomeric {[MgL 2 (H 2 O) 4 ] [L = 2-(2-fluorophenoxy)acetate (Kennard et al, 1986) and L = MCPA À (Smith et al, 1981)] and [MgL(H 2 O) 5 ]ÁL [L = 2,4,5-T À (Smith et al, 1982)]} or polymeric {[MgL 2 (H 2 O) 2 ]} n [L = phenoxyacetate, (4-chlorophenoxy)acetate or (4-fluorophenoxy)acetate] (Smith et al, 1980;Smith, 2012) …”
Section: Chemical Contextmentioning
confidence: 99%