Cyclopentadienylindium(I)

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Cyclopentadienylindium(I)
Cyclopentadienylindium.png
Names
Other names
indium cyclopentadienyl, cyclopentadienyl indium
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.222.670 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
  • InChI=1S/C5H5.In/c1-2-4-5-3-1;/h1-5H;
    Key: JZPXQBRKWFVPAE-UHFFFAOYSA-N
  • [In+].c1[cH-]ccc1
Properties
C5H5In
Molar mass 179.913 g/mol
Appearanceoff-white solid
Hazards
GHS labelling:
GHS-pictogram-flamme.svg GHS-pictogram-exclam.svg
Warning
H228, H302, H315, H319, H335
P210, P240, P241, P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P370+P378, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Cyclopentadienylindium(I), C5H5In, is an organoindium compound containing indium in the +1 oxidation state. Commonly abbreviated to CpIn, it is a cyclopentadienyl complex with a half-sandwich structure. It was the first (1957 [1] ) low-valent organoindium compound reported.

Contents

Preparation and chemistry

CpIn can be readily prepared by reacting indium(I) chloride with cyclopentadienyllithium: [2]

InCl + CpLi → CpIn + LiCl

InCp reacts with BF3, BCl3, BBr3, BI3 and trimethylborane B(CH3)3 to form adducts, [3] e.g.:

CpIn + BF3 → CpIn·BF3

In these adducts the bonding of the Cp ligand to the indium atom changes from η 5 (π complexing) to η1 (σ bonding).

Salts containing the InX2 anion containing indium in the +1 oxidation state have been prepared from cyclopentadieneindium; for example: [4]

CpIn + HCl + N(Et4)Cl → N(Et4)InCl2+ C5H6

Structure and bonding

Solid CpIn is polymeric consisting of zigzag chains of alternating indium atoms and C5H5 units. Two indium atoms interact with the opposite faces of each C5H5 ring, nearly perpendicularly to the ring plane, and two rings interact with each indium atom, forming an angle of about 128°. [5] In the CpIn monomer present in the vapour phase the indium atom sits on the central axis of the aromatic cyclopentadienyl anion, C5H5.

Bonding studies have shown that the aromatic ring electrons of the cyclopentadienyl anion interact with the indium 5s and 5p atomic orbitals, and that the lone pair on the indium atom is a dominant feature. [6]

InCp-chain-3D-balls.png
InCp-chain-3D-vdW.png
Ball-and-stick and space-filling models of CpIn chains
in the crystal structure of cyclopentadienylindium(I)

Related Research Articles

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A metallocene is a compound typically consisting of two cyclopentadienyl anions (C
5
H
5
, abbreviated Cp) bound to a metal center (M) in the oxidation state II, with the resulting general formula (C5H5)2M. Closely related to the metallocenes are the metallocene derivatives, e.g. titanocene dichloride or vanadocene dichloride. Certain metallocenes and their derivatives exhibit catalytic properties, although metallocenes are rarely used industrially. Cationic group 4 metallocene derivatives related to [Cp2ZrCH3]+ catalyze olefin polymerization.

Ferrocene is an organometallic compound with the formula Fe(C5H5)2. The molecule is a complex consisting of two cyclopentadienyl rings sandwiching a central iron atom. It is an orange solid with a camphor-like odor that sublimes above room temperature, and is soluble in most organic solvents. It is remarkable for its stability: it is unaffected by air, water, strong bases, and can be heated to 400 °C without decomposition. In oxidizing conditions it can reversibly react with strong acids to form the ferrocenium cation Fe(C5H5)+2. Ferrocene and the ferrocenium cation are sometimes abbreviated as Fc and Fc+ respectively.

Cyclopentadiene is an organic compound with the formula C5H6. It is often abbreviated CpH because the cyclopentadienyl anion is abbreviated Cp.

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<span class="mw-page-title-main">Nickelocene</span> Chemical compound

Nickelocene is the organonickel compound with the formula Ni(η5-C5H5)2. Also known as bis(cyclopentadienyl)nickel or NiCp2, this bright green paramagnetic solid is of enduring academic interest, although it does not yet have any known practical applications.

<span class="mw-page-title-main">Hapticity</span> Number of contiguous atoms in a ligand that bond to the central atom in a coordination complex

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<span class="mw-page-title-main">Chromocene</span> Chemical compound

Chromocene is the organochromium compound with the formula [Cr(C5H5)2]. Like structurally related metallocenes, chromocene readily sublimes in a vacuum and is soluble in non-polar organic solvents. It is more formally known as bis(η5-cyclopentadienyl)chromium(II).

<span class="mw-page-title-main">Tris(pentafluorophenyl)borane</span> Chemical compound

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<span class="mw-page-title-main">Decamethyldizincocene</span> Chemical compound

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In organometallic chemistry, a transition metal indenyl complex is a coordination compound that contains one or more indenyl ligands. The indenyl ligand is formally the anion derived from deprotonation of indene. The η5-indenyl ligand is related to the η5cyclopentadienyl anion (Cp), thus indenyl analogues of many cyclopentadienyl complexes are known. Indenyl ligands lack the 5-fold symmetry of Cp, so they exhibit more complicated geometries. Furthermore, some indenyl complexes also exist with only η3-bonding mode. The η5- and η3-bonding modes sometimes interconvert.

<span class="mw-page-title-main">Sodium cyclopentadienide</span> Chemical compound

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<span class="mw-page-title-main">Rhodocene</span> Organometallic chemical compound

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3
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References

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