| 1. | It is an example of a chiral diphosphine used in asymmetric hydrogenation.
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| 2. | It is classified as a diphosphine ligand in coordination chemistry and homogeneous catalysis.
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| 3. | It can be generated from diphosphine but is highly unstable at room temperature:
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| 4. | The application of diphosphine ligands to catalysts is not limited to the process of hydroformylation.
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| 5. | The compound is used as a bulky and highly basic diphosphine ligand in coordination chemistry.
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| 6. | Diphosphine ligands with bite angles of over 120?are obtained using a bulky, stiff diphosphine backbones.
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| 7. | Diphosphine ligands with bite angles of over 120?are obtained using a bulky, stiff diphosphine backbones.
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| 8. | "' Chiraphos "'is a diphosphine employed as a ligand in organometallic chemistry.
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| 9. | The bite angle of a diphosphine ligand also indicates the distortion from the ideal geometry of a complex based on VSEPR models.
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| 10. | Henri Kagan developed DIOP, an easily prepared C 2-symmetric diphosphine that gave high ee's in certain reactions.
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