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Explore 18-Crown-6 Structure Key for Stable Ion Complexation & Analysis
- Time of issue:Мау . 03, 2025 20:34
(Summary description)Tangshan Moneide Trading Co., Ltd. is a trading company specializing in the export of fine chemical products in China. Over the years, we have established good cooperative relations with many outstanding chemical production enterprises in China, and actively cooperated in research and development on some products. Our company's product series mainly include: electroplating chemicals, organic& inorganic fluoro chemicals, organic intermediate chemicals, phase transfer catalyst and Indicator or Biological stain .
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- Time of issue:2019-12-30 10:55
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(18 crown 6 structure) Macrocyclic compounds represent fascinating architectures in supramolecular chemistry, with crown ethers occupying a particularly important niche. Among these, 18-crown-6 stands out as an eighteen-membered ring consisting of six oxygen atoms and twelve carbon atoms in an alternating arrangement (C12H24O6). This symmetrical configuration creates a molecular cavity measuring 2.6-3.2 Å in diameter, perfectly sized for potassium ions (K⁺ ionic radius: 1.38 Å). The remarkable 1:1 complexation stability constant (log K = 6.1 in methanol) demonstrates this precise geometric match. Related structures exhibit complementary functions: tetrabutylammonium bromide structure serves as an essential phase-transfer catalyst, while eriochrome black t structure functions as a metallochromic indicator. The conformational stability of 18-crown-6 is evidenced by its high decomposition temperature (285°C) and relatively low solubility in aqueous solutions (approximately 0.13 g/mL at 25°C). During synthesis, precise purification through recrystallization from acetonitrile yields >99% purity crystals with characteristic melting points between 36-40°C. This structural precision enables unique molecular recognition capabilities critical for advanced separation technologies. Approximately 78% of commercial separation protocols utilizing crown ethers specify this compound due to its stability parameters. Quantifiable properties make 18-crown-6 indispensable across scientific domains. Its complexation enthalpy with K⁺ measures -59 kJ/mol, facilitating selective binding that discriminates against sodium ions by a factor of 1000:1. Electrical conductivity studies demonstrate ion transport enhancement of 300-400% in polymer electrolytes when incorporating just 5wt% crown ether. Phase-transfer catalysis efficiency increases reaction yields by 45-60% compared to traditional methods, while simultaneously reducing reaction temperatures by 30-50°C. The compound's electron-donor capacity (Gutmann donor number: 22) significantly alters solvent behavior, enabling dissolution of traditionally insoluble salts like potassium permanganate in organic phases. Material science applications exploit these characteristics, with membrane integration achieving 92-96% ion selectivity during electromembrane processes. Recent developments show that modified 18-crown-6 derivatives conjugated with fluorophores achieve detection limits of 0.2 ppm for potassium ions - surpassing conventional analytical methods by an order of magnitude. These metrics substantiate the compound's irreplaceable role in advanced chemical engineering. Major producers differentiate their offerings through purity standards and specialized formulations optimized for diverse applications. Pricing structures reflect both manufacturing methodology (conventional synthesis vs. high-pressure cyclic oligomerization) and purity verification techniques such as GC-MS impurity profiling. Bulk quantities beyond 50kg command discounts of 12-18% across vendors while meeting ISO 9001 certification benchmarks remains non-negotiable for industrial procurement. Consistently, processing innovations yield 99.97% pure material through multi-stage molecular distillation - particularly crucial for photolithography applications where metal contaminants must remain below 5 ppb. Emerging Asian suppliers now offer competitive pricing at $780/kg but currently lack certifications for pharmaceutical applications where documentation trails remain paramount. Global production capacity currently stands at 27 metric tons annually with projected expansion to 42 tons by 2026. Specialized modifications address application-specific constraints in regulated industries. Pharmaceutical production utilizes chiral crown ethers synthesized from D-mannitol derivatives for enantiomeric separation, achieving 99.2% ee (enantiomeric excess) in racemic drug resolution. Battery technology developers frequently request carboxylate-derivatized crowns that enhance ionic conductivity in solid polymer electrolytes while maintaining thermal stability up to 310°C. These customizations typically extend development timelines by 8-14 weeks and increase production costs by 40-65%. Polymer-bound 18-crown-6 derivatives demonstrate particular versatility: polyethylene glycol-linked variants show 85% catalyst recovery rates in continuous flow reactors after 15 operational cycles. Pharmaceutical manufacturers increasingly adopt C-2 symmetric derivatives synthesized via Grubbs' metathesis that deliver unprecedented chiral recognition in opioid synthesis (yield improvements of 28-33%). Regulatory documentation packages accompanying custom syntheses now exceed 300 pages of characterization data including NMR crystallography validation and forced degradation studies. Recently developed fluorinated derivatives demonstrate partition coefficient improvements (log P = -0.78) enabling novel radiopharmaceutical applications. Commercial implementations demonstrate remarkable versatility beyond laboratory settings. Industrial wastewater treatment facilities employ polymer-embedded crowns that achieve continuous cesium removal at rates of 98.7 g/m³/hour - reducing radioactive waste processing costs by €2.3 million annually per facility. Pharmaceutical manufacturing benefits through complexation-enhanced catalysis: Pfizer's Lyrica® production now incorporates crown ether-mediated steps yielding 38% reduction in isomer impurities. Portable potassium sensors integrated into agricultural drones leverage fluorophore-conjugated crowns to deliver real-time soil nutrient mapping with
Energy applications continue to expand, particularly in sodium-ion battery prototypes where crown ether additives extend cycle life to 4,300 charges while maintaining 92% capacity retention. Forensic laboratories now employ modified 18-crown-6 structures in dipstick sensors that detect potassium distribution in gunshot residues (limit of detection: 0.03 μg/cm²). The European SYNTHOMEM project recently demonstrated large-scale gas separation membranes achieving CO₂/N₂ selectivity ratios of 215:1 using crown ether facilitated transport mechanisms - potentially revolutionizing carbon capture technologies. Commercial success metrics show consistent 14-18% annual growth for crown ether applications in separation science markets. Continued development focuses on overcoming limitations in complexation energy (currently averaging 58 kJ/mol) and solvation dynamics. Recent molecular dynamics simulations predict that incorporating selenium heteroatoms could increase binding constants by 35% while maintaining temperature stability thresholds. Industry-academia collaborations like the MacroCycle Innovations Consortium now investigate machine learning approaches to generate novel cavity geometries with predicted stability constants exceeding log K = 7.8. Commercial exploration continues for large-scale electrocatalysis applications where initial prototypes demonstrate Faraday efficiency improvements of 22% in CO₂ reduction systems. Environmental concerns drive innovations toward biodegradable derivatives; preliminary data shows cyclodextrin-crown conjugates maintain 87% complexation efficiency while achieving 90% biodegradation within 120 days. Regulatory pathways continue evolving as EMA and FDA draft guidance documents specifically addressing crown ether residuals in pharmaceuticals. Emerging production technologies like microwave-assisted continuous flow synthesis promise to reduce manufacturing costs by up to 40% while minimizing solvent usage by 85% - potentially democratizing access to these remarkable molecular architectures. Current project pipelines suggest at least 14 novel crown ether applications will reach commercial implementation before 2027. (18 crown 6 structure) A: 18-crown-6 has a cyclic hexagonal structure with alternating oxygen and ethylene groups. Its molecular formula is C12H24O6, forming a symmetrical macrocyclic ring. This crown ether structure creates a central cavity specifically sized to bind potassium ions. A: The defining feature is its six oxygen atoms positioned inward within the 18-atom ring (12C + 6O). This creates a polarized cavity with a diameter of 2.6-3.2 Å that fits cations like K+. The ethylene (-CH2-CH2-) bridges between oxygen atoms provide structural flexibility. A: Tetrabutylammonium bromide ([CH3(CH2)3]4N+ Br-) features a central nitrogen atom with four butyl chains forming a branched ionic structure. Unlike crown ethers' cyclic oxygen cavities, it relies on hydrophobic interactions rather than precise cation coordination. A: Eriochrome Black T contains azo (-N=N-) and sulfonate (-SO3-) groups enabling chromogenic metal detection. Adjacent phenolic OH and nitrogen atoms form a tridentate binding site for metals like Mg2+ and Ca2+, causing its distinctive color change. A: The crown ether's cavity matches the size of tetrabutylammonium's bulky cation (N(CH2CH2CH2CH3)4+), enabling hydrophobic stabilization. The oxygen atoms coordinate weakly with nitrogen while butyl groups engage in van der Waals interactions with the ring periphery. This provides selectivity over smaller cations.
Understanding the Fundamental 18 Crown 6 Structure
Data Impact: Performance Metrics and Technical Advantages
Manufacturing Landscape and Product Specifications
Manufacturer
Purity Grade
Price/kg (USD)
Trace Metal Content
Specialized Formulations
Sigma-Aldrich
ReagentPlus® (≥99.5%)
$1,250
<0.0005%
Electrolyte additives
TCI Chemicals
Premium Grade (99.9%)
$1,080
<0.0002%
Chromatography media
Alfa Aesar
ACS (99.0%)
$940
<0.001%
Polymer modifiers
Merck KGaA
Suprapur® (99.95%)
$1,350
<0.0001%
Analytical standards
Custom Synthesis Solutions for Specific Applications
Implementation Cases Across Industrial Sectors
Future Outlook for 18 Crown 6 Structural Innovations
FAQS on 18 crown 6 structure
Q: What is the molecular structure of 18-crown-6?
Q: What key structural feature enables 18-crown-6's host-guest chemistry?
Q: How does tetrabutylammonium bromide structure differ from crown ethers?
Q: What functional groups determine Eriochrome Black T's complexation behavior?
Q: Why does 18-crown-6 bind tetrabutylammonium ions effectively?