Bis(dinitrogen)bis­(1,2-bis(diphenylphosphino)­ethane)molybdenum(0)
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
59731
  • InChI=1S/2C26H24P2.Mo.2N2/c2*1-5-13-23(14-6-1)27(24-15-7-2-8-16-24)21-22-28(25-17-9-3-10-18-25)26-19-11-4-12-20-26;;2*1-2/h2*1-20H,21-22H2;;;
    Key: ZEYRIXZZLVGNMH-UHFFFAOYSA-N
  • P(c1ccccc1)(c2ccccc2)CCP(c3ccccc3)c4ccccc4.P(c5ccccc5)(c6ccccc6)CCP(c7ccccc7)c8ccccc8.N#N.N#N.[Mo]
Properties
C52H48MoN4P4
Molar mass 948.84
Appearance Yellow-orange crystals[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

trans-Bis(dinitrogen)bis[1,2-bis(diphenylphosphino)ethane]molybdenum(0) is a coordination complex with the formula Mo(N2)2(dppe)2. It is a relatively air stable yellow-orange solid. It is notable as being the first discovered dinitrogen containing complex of molybdenum.[1]

Structure

Mo(N2)2(dppe)2 is an octahedral complex with idealized D2h point group symmetry. The dinitrogen ligands are mutually trans across the metal center. The Mo-N bond has a length of 2.01 Å, and the N-N bond has a length of 1.10 Å.[2] This length is close to the free nitrogen bond length, but coordination to the metal weakens the N-N bond making it susceptible to electrophilic attack.[3]

Synthesis

The first synthetic route to Mo(N2)2(DPPE)2 involved a reduction of molybdenum(III) acetylacetonate with triethylaluminium in the presence of dppe and nitrogen.

A higher yielding synthesis involves a four-step process.[4] In the first step, molybdenum(V) chloride is reduced by acetonitrile (CH3CN) to give [MoCl4(CH3CN)2]. Acetonitrile is displaced by tetrahydrofuran (THF) to give [MoCl4(THF)2]. This Mo(IV) compound is reduced by tin powder to [MoCl3(thf)3]. The desired compound is formed in the presence of nitrogen gas, dppe ligand, and magnesium turnings as the reductant:

3 Mg + 2 MoCl3(THF)3 + 4 Ph2PCH2CH2PPh2 + 4 N2 → 2 trans-[Mo(N2)2(Ph2PCH2CH2PPh2)2] + 3 MgCl2 + 6 THF

Reactivity

The terminal nitrogen is susceptible to electrophilic attack, allowing for the fixation of nitrogen to ammonia in the presence of acid. In this way, Mo(N2)2(dppe)2 serves as a model for biological nitrogen fixation. Carbon-nitrogen bonds can also be formed with this complex through condensation reactions with ketones and aldehydes, and substitution reactions with acid chlorides. The terminal nitrogen can also be silylated.[3]

See also

References

  1. 1 2 Hidai, Masanobu.; Mizobe, Yasushi. (1995). "Recent Advances in the Chemistry of Dinitrogen Complexes". Chemical Reviews. 95 (4): 1115. doi:10.1021/cr00036a008.
  2. ↑ Uchida, Tokiko; Uchida, Yasuzo; Hidai, Masanobu; Kodama, Teruyuki (1971). "The Crystal and Molecular Structure oftrans-Bis(dinitrogen)bis[1,2-bis(diphenylphosphino)ethane]molybdenum(0)". Bulletin of the Chemical Society of Japan. 44 (10): 2883. doi:10.1246/bcsj.44.2883.
  3. 1 2 Hidai, Masanobu; Mizobe, Yasushi (1993). "Chemical Transformations of Coordinated Dinitrogen in Molybdenum and Tungsten Phosphine Complexes". Molybdenum Enzymes, Cofactors, and Model Systems. ACS Symposium Series. Vol. 535. pp. 346. doi:10.1021/bk-1993-0535.ch022. ISBN 0-8412-2708-X.
  4. ↑ Jonathan R. Dilworth; Raymond L. Richards (1990). The Synthesis of Molybdenum and Tungsten Dinitrogen Complexes. Inorganic Syntheses. Vol. 28. pp. 33–45. doi:10.1002/9780470132593.ch7. ISBN 9780470132593.
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