Self-Assembly of Manganese(II)-Phytate Coordination Polymers: Synthesis, Crystal Structure, and Physicochemical Properties.

Chempluschem

Departamento Estrella Campos, Facultad de Química, Universidad de la República, General Flores 2124, Montevideo, Uruguay.

Published: May 2017

myo-Inositol phosphates are an important group of biomolecules that are present in all eukaryotic cells. The most abundant member of this family in nature is InsP (phytate, L in its fully deprotonated form). Phytate interacts strongly with inorganic and organic cations, and this interaction is essential for determining the possible functions of this biomolecule. Herein, the chemical, thermodynamic, and structural characterization of phytate-Mn species is presented in a study aimed at understanding how the interaction of the two components modulates their biological roles and their bioavailability. Polynuclear complexes Mn (H L)⋅16 H O (1) and (H terpy) [Mn(H L)(terpy)(H O)]⋅17 H O (terpy=terpyridine) (2) were prepared and characterized by different techniques. The isolation of 1 and the determination of its solubility, together with potentiometric titrations of the Mn -phytate system, allow the full description of this binary system. The preparation and crystal structure of 2 show a novel coordination mode of phytate, that is, the formation of infinite polymeric chains through equatorial phosphate groups.

Download full-text PDF

Source
http://dx.doi.org/10.1002/cplu.201700027DOI Listing

Publication Analysis

Top Keywords

crystal structure
8
self-assembly manganeseii-phytate
4
manganeseii-phytate coordination
4
coordination polymers
4
polymers synthesis
4
synthesis crystal
4
structure physicochemical
4
physicochemical properties
4
properties myo-inositol
4
myo-inositol phosphates
4

Similar Publications

The matere bond.

Dalton Trans

January 2025

Department of Chemistry, Universitat de les Illes Balears, Crta de Valldemossa km 7.5, 07122 Palma de Mallorca, Baleares, Spain.

This perpective delves into the emerging field of matere bonds, a novel type of noncovalent interaction involving group 7 elements such as manganese, technetium, and rhenium. Matere bonds, a new member of the σ-hole family where metal atoms act as electron acceptors, have been shown experimentally and theoretically to play significant roles in the self-assembly and stabilization of supramolecular structures both in solid-state and solution-phase environments. This perspective article explores the physical nature of these interactions, emphasizing their directionality and structural influence in various supramolecular architectures.

View Article and Find Full Text PDF

Monoprotonated species of 2-aminomalonyl difluoride, [CHFNO][HF].

Acta Crystallogr C Struct Chem

February 2025

Department Chemie, Ludwig-Maximilians Universität, Butenandtstrasse 5-13 (Haus D), D-81377 München, Germany.

The monoprotonated species of 2-aminomalonyl difluoride, namely, 1,3-difluoro-1,3-dioxopropan-2-aminium dihydrogen trifluoride, [CHFNO][HF], was synthesized from sulfur tetrafluoride in anhydrous hydrogen fluoride (aHF) with [NH][CHNO] as the starting material. The solvent was removed and the salt was dissolved in aHF and crystallized. In the solid state, the three-dimensional network is built by medium-strong N-H.

View Article and Find Full Text PDF

In this work, coixalkyne A (), a natural polynuclear calcium complex with a novel cross-shaped molecular architecture, was isolated from L. along with the undescribed analogue coixalkyne B (). Their structures were identified by means of NMR spectroscopy, ECD calculations, and single-crystal X-ray diffraction.

View Article and Find Full Text PDF

Steam explosion (SE) and cellulase treatment are potentially effective processing methods for by-products, for use in high-value applications. The treatment conditions were optimized by response surface methodology, increasing the soluble dietary fiber (SDF) yield by 1.52 and 1.

View Article and Find Full Text PDF

The layer-stacking mode of a two-dimensional (2D) material plays a dominant role either in its topology or properties, but remains challenging to control. Herein, we developed alkali-metal ion-regulating synthetic control on the stacking structure of a vinylene-linked covalent triazine framework (termed spc-CTF) for improving hydrogen peroxide (HO) photoproduction. Upon the catalysis of EtONa in Knoevenagel polycondensation, a typical eclipsed stacking mode (spc-CTF-4@AA) was built, while a staggered one (spc-CTF-4@AB) was constructed using LiOH.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!