Synthesis, characterization and anti‐microbial studies of cadmium(II) compounds containing 3,10‐C‐meso‐Me8[14]aneC. Crystal and molecular structure of cis‐[CdLC(NO3)](NO3)
Abstract:− ligand is replaced by two monodentate ligands that occupy axial positions. All compounds were characterized on the basis of analytical, spectroscopic, conductometric and magnetochemical data. The crystal structure of cis-CdL C (NO 3 )](NO 3 ) was determined by X-ray crystallography and showed the cadmium centre to exist within a cis-N 4 O 2 donor set that defined a distorted octahedral geometry. Non-systematic variations in the Cd-O and Cd-N bond distances were correlated with significant hydrogen bonding in… Show more
“…The latter value is longer than the sum of ionic radii (Cd 2+ CN7 : 1.03 Å; O 2– : 1.35 Å). Similar values were reported for CdN 4 O 3 in the CTP environment, and as expected, the Cd–O bond to the capping O 2– is longer than to O 2– anions in the trigonal prism. − The Cd–N bonds are between 2.196 and 2.485 Å (Table S8), in agreement with literature values. − The N–Cd–N and O–Cd–O cis angles range from 74.4(4)° to 97.9(4)°, respectively, from 62.96(14)° to 65.78(14)°, and the N–Cd−μ 2 -O angles are 74.2(3)–96.8(3)°. The trans angles cover a wide range as expected by different orientations of the monocapped trigonal prisms (Table S9), but the geometric parameters are not unusual and similar data were reported in the literature. ,, …”
Diffusion-based
room temperature syntheses using K8{Ta6O19}·16H2O, d-block metal (M) salts
(M = Cu, Zn, or Cd), and the macrocyclic ligand 1,4,8,11-tetraazacyclotetradecane
(cyclam) led to crystallization of the three new polyoxotantalates
with the composition K4{[Cu(cyclam)]2Ta6O19}·18H2O (I), K4{[Zn(cyclam)]2Ta6O19}·18H2O (II), and {[Cd(cyclam)]4Ta6O19}·19H2O (III). The latter
two compounds represent the first polyoxotantalates (POTas) with Zn2+ and Cd2+ centered amine complexes and also the
first POTas synthesized using a macrocyclic amine. Compounds I and II are isostructural with two complexes
attached to the anionic cluster via Cu–O–Ta respectively
Zn–O–Ta bonds. Despite that these two compounds are
isostructural, the geometry of the M2+ complexes differs
significantly with Cu2+ in a square-pyramidal and Zn2+ in a trigonal-bipyramidal environment. In the structure
of III, the Cd2+ cations are in the rare hepta-coordinated
monocapped trigonal prismatic geometry covalently linked to the anionic
core via Cd–O–Ta bonds. While compounds I and II are quite stable under ambient conditions, III shows a fast loss of crystal water molecules. Temperature-dependent
in situ XRD measurements were performed with I demonstrating
stepwise structural rearrangements caused by water release.
“…The latter value is longer than the sum of ionic radii (Cd 2+ CN7 : 1.03 Å; O 2– : 1.35 Å). Similar values were reported for CdN 4 O 3 in the CTP environment, and as expected, the Cd–O bond to the capping O 2– is longer than to O 2– anions in the trigonal prism. − The Cd–N bonds are between 2.196 and 2.485 Å (Table S8), in agreement with literature values. − The N–Cd–N and O–Cd–O cis angles range from 74.4(4)° to 97.9(4)°, respectively, from 62.96(14)° to 65.78(14)°, and the N–Cd−μ 2 -O angles are 74.2(3)–96.8(3)°. The trans angles cover a wide range as expected by different orientations of the monocapped trigonal prisms (Table S9), but the geometric parameters are not unusual and similar data were reported in the literature. ,, …”
Diffusion-based
room temperature syntheses using K8{Ta6O19}·16H2O, d-block metal (M) salts
(M = Cu, Zn, or Cd), and the macrocyclic ligand 1,4,8,11-tetraazacyclotetradecane
(cyclam) led to crystallization of the three new polyoxotantalates
with the composition K4{[Cu(cyclam)]2Ta6O19}·18H2O (I), K4{[Zn(cyclam)]2Ta6O19}·18H2O (II), and {[Cd(cyclam)]4Ta6O19}·19H2O (III). The latter
two compounds represent the first polyoxotantalates (POTas) with Zn2+ and Cd2+ centered amine complexes and also the
first POTas synthesized using a macrocyclic amine. Compounds I and II are isostructural with two complexes
attached to the anionic cluster via Cu–O–Ta respectively
Zn–O–Ta bonds. Despite that these two compounds are
isostructural, the geometry of the M2+ complexes differs
significantly with Cu2+ in a square-pyramidal and Zn2+ in a trigonal-bipyramidal environment. In the structure
of III, the Cd2+ cations are in the rare hepta-coordinated
monocapped trigonal prismatic geometry covalently linked to the anionic
core via Cd–O–Ta bonds. While compounds I and II are quite stable under ambient conditions, III shows a fast loss of crystal water molecules. Temperature-dependent
in situ XRD measurements were performed with I demonstrating
stepwise structural rearrangements caused by water release.
“…Relevant to the present study are recent reports describing the antibacterial activities of cadmium compounds [11,12,13,14]. These follow earlier studies, whereby cadmium(II) macrocyclic compounds were reported to exhibit potent antibacterial potential [13,14]. In addition, we have also reported x-ray crystallographic studies of cadmium(II) compounds with other macrocycles [14,15].…”
Section: Introductionsupporting
confidence: 82%
“…Due to the multifarious applications [1,2,3,4,5,6,7,8,9,10] of macrocyclic ligands, including differential behavior exhibited by their isomeric forms and their metal complexes in a wide variety of contexts, researchers continue to be fascinated by their chemistry and various applications, including in the development of metal-based drugs and as imaging agents. Relevant to the present study are recent reports describing the antibacterial activities of cadmium compounds [11,12,13,14]. These follow earlier studies, whereby cadmium(II) macrocyclic compounds were reported to exhibit potent antibacterial potential [13,14].…”
Section: Introductionsupporting
confidence: 81%
“…These follow earlier studies, whereby cadmium(II) macrocyclic compounds were reported to exhibit potent antibacterial potential [13,14]. In addition, we have also reported x-ray crystallographic studies of cadmium(II) compounds with other macrocycles [14,15]. Though copper(II), nickel(II), and cobalt(III), and chromium(III) complexes of macrocyclic ligands described herein have been reported [16,17], related studies on cadmium(II) have yet to be reported.…”
Section: Introductionsupporting
confidence: 79%
“…
The isomeric ligand L C , a saturated analogue of 2,9-C-meso-Me 8 [14]diene, on reflux with excess acrylonitrile afforded 1,8-N-pendant cyanoethyl derivative L CX . Interaction of L CX with cadmium(II) perchlorate, nitrate, acetate, and chloride salts produced six coordinated octahedral compounds,, and [Cd(L CX )Cl 2 ], respectively.
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