Allylchloro-[1,3-bis-(2,6-diisopropylphenyl)-2-imidazolidinylidene]palladium(II)
Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II)
CAS: 478980-01-7
Molecular Formula: C30H40ClN2Pd
Allylchloro-[1,3-bis-(2,6-diisopropylphenyl)-2-imidazolidinylidene]palladium(II) - Names and Identifiers
Allylchloro-[1,3-bis-(2,6-diisopropylphenyl)-2-imidazolidinylidene]palladium(II) - Physico-chemical Properties
| Molecular Formula | C30H40ClN2Pd |
| Molar Mass | 570.53 |
| Melting Point | 206-210°C |
| Appearance | Powder |
| Color | white |
| Storage Condition | 2-8°C |
Allylchloro-[1,3-bis-(2,6-diisopropylphenyl)-2-imidazolidinylidene]palladium(II) - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| WGK Germany | 3 |
| HS Code | 28439000 |
Allylchloro-[1,3-bis-(2,6-diisopropylphenyl)-2-imidazolidinylidene]palladium(II) - Introduction
Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) is an organic compound with the chemical formula C36H47ClN2Pd. It is a coordination compound and has the following properties:
1. Appearance: Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) is a solid with yellow or orange crystals.
2. Stability: The compound is relatively stable under dry conditions, but may decompose in humid and oxidizing environments.
The main uses of Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) include:
1. Catalyst: As a homogeneous catalyst, Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) can catalyze the formation of C- C bonds in organic synthesis reactions, such as Suzuki coupling reaction and Heck reaction.
2. Cross-coupling reaction: The compound is often used in cross-coupling reactions in organic synthesis, and can effectively construct complex organic molecular frameworks.
The preparation method of Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) is generally obtained by the synthesis of a coordination compound and the addition reaction of palladium chloride. The specific preparation method can be carried out according to specific literature or laboratory methods.
Regarding safety information, the safety of Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) needs more detailed research. During use, please follow the safe operation procedures for chemicals, avoid direct contact with skin and eyes, and ensure that you operate under well-ventilated conditions. Wear appropriate personal protective equipment if necessary.
1. Appearance: Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) is a solid with yellow or orange crystals.
2. Stability: The compound is relatively stable under dry conditions, but may decompose in humid and oxidizing environments.
The main uses of Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) include:
1. Catalyst: As a homogeneous catalyst, Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) can catalyze the formation of C- C bonds in organic synthesis reactions, such as Suzuki coupling reaction and Heck reaction.
2. Cross-coupling reaction: The compound is often used in cross-coupling reactions in organic synthesis, and can effectively construct complex organic molecular frameworks.
The preparation method of Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) is generally obtained by the synthesis of a coordination compound and the addition reaction of palladium chloride. The specific preparation method can be carried out according to specific literature or laboratory methods.
Regarding safety information, the safety of Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II) needs more detailed research. During use, please follow the safe operation procedures for chemicals, avoid direct contact with skin and eyes, and ensure that you operate under well-ventilated conditions. Wear appropriate personal protective equipment if necessary.
Last Update：2024-04-10 22:29:15
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