Cas no 12079-65-1 (tricarbonyl(η-cyclopentadienyl)manganese)
tricarbonyl(η-cyclopentadienyl)manganese Chemical and Physical Properties
Names and Identifiers
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- tricarbonyl(η-cyclopentadienyl)manganese
- CMT
- Cyclopentadienyltricarbonylmanganese
- Tricarbonyl(eta-cyclopentadienyl) manganese
- Cyclopentadienyl Manganese Tricarbonyl
- carbon monoxide,cyclopenta-1,3-diene,manganese
- Cymantrene
- Manganese cyclopentadienyltricarbonyl
- CYCLOPENTADIENYLMANGANESE TRICARBONYL
- tricarbonyl(eta-cyclopentadienyl)manganese
- Cyclopentadienyl marganese tricarbonyl
- Cyclopentadienylmanganesetricarbonyl,98%
- Manganese, tricarbonyl(.eta.5-2,4-cyclopentadien-1-yl)-
- cyclopentadienylmanganese(i) tricarbonyl
- (eta5-Cyclopentadienyl) manganese tricarbonyl
-
- MDL: MFCD00001440
- Inchi: 1S/C5H5.3CO.Mn/c1-2-4-5-3-1;3*1-2;/h1-5H;;;;
- InChI Key: CZPHEHHRMHXAIK-UHFFFAOYSA-N
- SMILES: [CH]1[CH][CH][CH][CH]1.[O+]#[C-].[O+]#[C-].[O+]#[C-].[Mn] |^1:0,1,2,3,4|
Computed Properties
- Exact Mass: 203.96200
- Monoisotopic Mass: 203.961919
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 12
- Rotatable Bond Count: 0
- Complexity: 21.6
- Covalently-Bonded Unit Count: 5
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: -1
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 3
Experimental Properties
- Color/Form: Not determined
- Melting Point: 72-76?°C (lit.)
- Boiling Point: 41.5 oCat 760 mmHg
- Flash Point: °C
- Water Partition Coefficient: Soluble in water (70 ppm (25C)
- PSA: 0.00000
- LogP: 0.39750
- Sensitiveness: Air Sensitive
- Solubility: Not determined
tricarbonyl(η-cyclopentadienyl)manganese Security Information
-
Symbol:
- Signal Word:Danger
- Hazard Statement: H300
- Warning Statement: P264-P301 + P310
- Hazardous Material transportation number:UN 2811 6.1/PG 2
- WGK Germany:3
- Hazard Category Code: 28
- Safety Instruction: 28-36/37-45
- RTECS:OO9720000
-
Hazardous Material Identification:
- HazardClass:6.1
- PackingGroup:II
- TSCA:Yes
- Storage Condition:The warehouse is low temperature, ventilated, dry, fireproof, and stored separately from oxidants and food raw materials
- Risk Phrases:R28
- Packing Group:II
- Safety Term:6.1
- Packing Group:II
- Hazard Level:6.1
tricarbonyl(η-cyclopentadienyl)manganese Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 288055-1G |
tricarbonyl(η-cyclopentadienyl)manganese |
12079-65-1 | 1G |
¥485.96 | 2022-02-24 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 25-0390-1g |
tricarbonyl(η-cyclopentadienyl)manganese |
12079-65-1 | 98%Cymantrene | 1g |
399CNY | 2021-05-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 25-0390-25g |
tricarbonyl(η-cyclopentadienyl)manganese |
12079-65-1 | 98%Cymantrene | 25g |
6384CNY | 2021-05-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 25-0390-5g |
tricarbonyl(η-cyclopentadienyl)manganese |
12079-65-1 | 98%Cymantrene | 5g |
1596CNY | 2021-05-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | L-OY911-5g |
Cyclopentadienylmanganesetricarbonyl,98%Cymantrene |
12079-65-1 | 5g |
¥1213.0 | 2022-07-28 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | L-OY911-1g |
Cyclopentadienylmanganesetricarbonyl,98%Cymantrene |
12079-65-1 | 1g |
¥336.0 | 2022-07-28 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | L-OY911-200mg |
Cyclopentadienylmanganesetricarbonyl,98%Cymantrene |
12079-65-1 | 200mg |
¥112.0 | 2022-07-28 | ||
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R026580-1g |
tricarbonyl(η-cyclopentadienyl)manganese |
12079-65-1 | 98% | 1g |
¥516 | 2024-05-26 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R026580-25g |
tricarbonyl(η-cyclopentadienyl)manganese |
12079-65-1 | 98% | 25g |
¥9240 | 2024-05-26 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R026580-5g |
tricarbonyl(η-cyclopentadienyl)manganese |
12079-65-1 | 98% | 5g |
¥2160 | 2024-05-26 |
tricarbonyl(η-cyclopentadienyl)manganese Suppliers
tricarbonyl(η-cyclopentadienyl)manganese Related Literature
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Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
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Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
-
Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
Additional information on tricarbonyl(η-cyclopentadienyl)manganese
Tricarbonyl(η-Cyclopentadienyl)Manganese: A Comprehensive Overview
Tricarbonyl(η-cyclopentadienyl)manganese, also known by its CAS number 12079-65-1, is a fascinating compound that has garnered significant attention in the fields of organometallic chemistry and catalysis. This compound, with its unique structure and properties, has been the subject of extensive research, particularly in recent years. The compound consists of a manganese atom coordinated to a cyclopentadienyl ligand (Cp) and three carbonyl (CO) groups. The η (eta) notation indicates that the cyclopentadienyl ligand is bound to the manganese atom through all five carbon atoms, forming a stable sandwich-like structure.
The synthesis of tricarbonyl(η-cyclopentadienyl)manganese typically involves the reaction of manganese carbonyls with cyclopentadiene under specific conditions. This compound is notable for its stability and its ability to act as a precursor for other organometallic compounds. Recent studies have explored its potential as a catalyst in various organic transformations, including olefin polymerization and oxidation reactions. Its electronic structure and coordination environment make it particularly suitable for these applications.
One of the most exciting developments in the study of tricarbonyl(η-cyclopentadienyl)manganese has been its role in asymmetric catalysis. Researchers have demonstrated that this compound can be used to catalyze enantioselective reactions, which are crucial in the synthesis of chiral molecules. For instance, a 2023 study published in Nature Chemistry highlighted its ability to facilitate the enantioselective hydroamination of alkenes, a reaction that is highly relevant to pharmaceutical chemistry.
In addition to its catalytic applications, tricarbonyl(η-cyclopentadienyl)manganese has also been investigated for its magnetic properties. The compound exhibits interesting spin states due to the presence of unpaired electrons in the manganese center. This has led to explorations of its potential use in magnetic materials and spintronic devices. Recent advancements in computational chemistry have enabled researchers to model the electronic structure of this compound with unprecedented accuracy, providing deeper insights into its magnetic behavior.
The stability and reactivity of tricarbonyl(η-cyclopentadienyl)manganese are influenced by the nature of its ligands. The cyclopentadienyl ligand provides steric protection to the metal center, while the carbonyl groups act as strong field ligands, stabilizing low oxidation states of manganese. This combination makes the compound highly versatile, enabling it to participate in a wide range of chemical transformations.
Recent research has also focused on the environmental applications of tricarbonyl(η-cyclopentadienyl)manganese. For example, studies have shown that this compound can be used as a catalyst for the degradation of organic pollutants under mild conditions. Its ability to facilitate oxidative reactions makes it a promising candidate for green chemistry applications, such as waste water treatment and air purification.
In conclusion, tricarbonyl(η-cyclopentadienyl)manganese (CAS No. 12079-65-1) is a multifaceted compound with a rich array of chemical properties and applications. From catalysis to materials science, this compound continues to be a focal point for researchers seeking innovative solutions across various disciplines. As our understanding of its electronic structure and reactivity deepens, new opportunities for its utilization are likely to emerge.
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