Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

EDTA: Chemistry and Properties01:22

EDTA: Chemistry and Properties

Polydentate ligands are most widely used in complexometric titrations because they form more stable complexes with the metal ions than mono- or bidentate ligands due to the chelate effect. Examples of polydentate ligands are ethylenediaminetetraacetic acid (EDTA), crown ethers, and cryptands. The most important feature of optimal polydentate ligands is the ability to form 1:1 complexes in a single-step process. Amino carboxylic acid derivatives are frequently used as complexing agents. EDTA is...
EDTA: Auxiliary Complexing Reagents01:26

EDTA: Auxiliary Complexing Reagents

EDTA titrations are usually carried out in highly basic conditions, where the fully deprotonated form of EDTA, Y4−, actively complexes with the free metal ions in the solution. Several metal ions precipitate as hydrous oxide (hydroxides, oxides, or oxyhydroxides) under these conditions, lowering the concentration of free metal ions in the solution. For this reason, auxiliary complexing agents or ligands such as ammonia, tartrate, citrate, or triethanolamine are used in EDTA titrations to...
Qualitative Analysis03:46

Qualitative Analysis

For solutions containing mixtures of different cations, the identity of each cation can be determined by qualitative analysis. This technique involves a series of selective precipitations with different chemical reagents, each reaction producing a characteristic precipitate for a specific group of cations. Metal ions within a group are further separated by varying the pH, heating the mixture to redissolve a precipitate, or adding other reagents to form complex ions.
For instance, group IV...
Formation of Complex Ions03:45

Formation of Complex Ions

A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
Masking and Demasking Agents01:19

Masking and Demasking Agents

EDTA titrations may necessitate masking and demasking agents to temporarily protect a particular metal ion in a mixture from the EDTA reaction. These agents facilitate the sequential analysis of the metal ions by forming stable complexes with some—but not all—metal ions during certain steps.
There are many masking agents, such as cyanide, fluoride, triethanolamine, thiourea, and 2,3-bis(sulfanyl)propan-1-ol (formerly 2,3-dimercapto-1-propanol), with the masking agent chosen based on the metal...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Correction: The relationship between built environment and mental health of older adults: mediating effects of perceptions of community cohesion and community safety and the moderating effect of income.

Frontiers in public health·2026
Same author

Tailoring the electronic structure of cobalt phthalocyanine on BiVO<sub>4</sub><i>via</i> substituent effects for enhancing photoelectrochemical water splitting.

Physical chemistry chemical physics : PCCP·2026
Same author

Mechanism of Anomalous Anisotropic Colossal Magnetoresistance in Quasi-2D Mn<sub>3</sub>Si<sub>2</sub>Te<sub>6</sub> Bulk Single Crystal.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2025
Same author

A two-stage transdermal drug delivery system comprising sono-phase-change transfersomes for non-invasive deep dermal delivery.

Journal of nanobiotechnology·2025
Same author

Fluoride-Mediated Synthesis of Co(OH)F and Electronic Structure Optimization for Enhanced Water Oxidation Performance.

Molecules (Basel, Switzerland)·2025
Same author

From Chinemys reevesii shell to trauma care: Preparation and characterization of chitosan-tortoiseshell collagen composite sponge with hemostasis property.

International journal of biological macromolecules·2025

Related Experiment Video

Updated: May 24, 2026

Synthesis of Cationized Magnetoferritin for Ultra-fast Magnetization of Cells
10:23

Synthesis of Cationized Magnetoferritin for Ultra-fast Magnetization of Cells

Published on: December 13, 2016

Oxymatrinium tetra-chloridoferrate(III).

Xiong He1, Xing Chuan Wei, Yu Chang Tian

  • 1School of Chemistry and Chemical Engineering, Guangzhou University, Guangzhou 510000, People's Republic of China.

Acta Crystallographica. Section E, Structure Reports Online
|February 21, 2012
PubMed
Summary

The crystal structure of an oxymatrinium cation with a tetrachloridoferrate(III) anion was determined. Hydrogen bonds link chiral oxymatrine cations into chains, revealing the compound's molecular arrangement.

More Related Videos

Stable Aqueous Suspensions of Manganese Ferrite Clusters with Tunable Nanoscale Dimension and Composition
10:45

Stable Aqueous Suspensions of Manganese Ferrite Clusters with Tunable Nanoscale Dimension and Composition

Published on: February 5, 2022

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron
07:56

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron

Published on: August 12, 2019

Related Experiment Videos

Last Updated: May 24, 2026

Synthesis of Cationized Magnetoferritin for Ultra-fast Magnetization of Cells
10:23

Synthesis of Cationized Magnetoferritin for Ultra-fast Magnetization of Cells

Published on: December 13, 2016

Stable Aqueous Suspensions of Manganese Ferrite Clusters with Tunable Nanoscale Dimension and Composition
10:45

Stable Aqueous Suspensions of Manganese Ferrite Clusters with Tunable Nanoscale Dimension and Composition

Published on: February 5, 2022

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron
07:56

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron

Published on: August 12, 2019

Area of Science:

  • Inorganic Chemistry
  • Crystallography
  • Organic Chemistry

Background:

  • Oxymatrine is a natural alkaloid with potential biological activities.
  • Understanding the solid-state structure of its derivatives is crucial for structure-activity relationship studies.

Purpose of the Study:

  • To determine the crystal structure of the oxymatrinium tetrachloridoferrate(III) compound.
  • To analyze the conformation and intermolecular interactions of the oxymatrinium cation.

Main Methods:

  • Single-crystal X-ray diffraction was used to elucidate the crystal structure.
  • Analysis of bond lengths, bond angles, and hydrogen bonding patterns.

Main Results:

  • The asymmetric unit contains one oxymatrinium cation and one tetrachloridoferrate(III) anion.
  • The oxymatrine conformation is similar to matrine, featuring chair and half-chair conformations.
  • Chiral chains of oxymatrinium cations are formed along the c-axis via O-H⋯O hydrogen bonds.

Conclusions:

  • The crystal structure provides insights into the solid-state behavior of oxymatrine derivatives.
  • Hydrogen bonding plays a significant role in organizing the molecular structure.
  • This study contributes to the understanding of alkaloid crystal engineering.