Metal Carbonyl Compounds. The first metal carbonyl compound described was Ni(CO) 4 (Ludwig Mond,...
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Transcript of Metal Carbonyl Compounds. The first metal carbonyl compound described was Ni(CO) 4 (Ludwig Mond,...
Metal Carbonyl Compounds
Lecture 16a
The first metal carbonyl compound described was Ni(CO)4 (Ludwig Mond, ~1890), which was used to refine nickel metal (Mond Process)
Ni(CO)4 is very volatile (b.p. =40 oC) and also very toxic!
Metal carbonyl compounds are used in many industrial processes producing organic compounds i.e., Monsanto process (acetic acid), Fischer Tropsch process (gasoline, ethylene glycol, methanol) or Reppe carbonylation (vinyl esters) from simple precursors (CO, CO2, H2, H2O)
Vaska’s complex (IrCl(CO)(PPh3)2) absorbs oxygen reversibly and serves as model for the oxygen absorption of myoglobin and hemoglobin (CO and Cl-ligand are disordered in the structure, two CO ligands are shown in the structure)
Introduction
Ni + 4 CO Ni(CO)4
50-60 oC
200-250 oC
Carbon monoxide is a colorless, tasteless gas that is highly toxic because it strongly binds to the iron in hemoglobin
The molecule is generally described with a triple bond because the bond distance of d=113 pm is too short for a double bond i.e., formaldehyde (H2C=O, d=121 pm)
The structure on the left is the major contributor because both atoms have an octet in this resonance structure (m=0.122 D)
The lone pair of the carbon atom is located in a sp-orbital
Carbon Monoxide
The CO ligand usually binds via the carbon atom to the metal
The lone pair on the carbon forms a s-bond with a suitable d-orbital of the metal (i.e., d(x2-y2))
The metal can form a p-backbond via the p*-orbital of theCO ligand (i.e., d(xy))
Electron-rich metals i.e., late transition metals in low oxidation states are more likely to donate electrons for the backbonding
A strong p-backbond results in a shorter the M-C bond and a longer the C-O (II) bond due to the population of an anti-bonding orbital in the CO ligand (see infrared spectrum)
Bond Mode of CO to Metals
xy-plane
(I) (II)
M C O M C O
Some compounds can be obtained by direct carbonylation of a metal at room temperature or elevated temperatures
In other cases, the metal has to be generated in-situ by reduction of a metal halide or metal oxide
Many polynuclear metal carbonyl compounds can be obtained using photochemistry which exploits the labile character of many M-CO bonds
Synthesis
Ni + 4 CO25 oC/1 atm
Ni(CO)4
Fe + 5 CO150 oC/100 atm
Fe(CO)5
CrCl3 + Al + 6 CO Cr(CO)6 + AlCl3
Re2O7 + 17 CO Re2(CO)10 + 7 CO2
2 Fe(CO)5
CH3COOH
UV-light
Fe2(CO)9 + CO
(CO)= 2057 cm -1
(CO)= 2013, 2034 cm -1
(CO)= 2000 cm -1
(CO)= 1983, 2013, 2044 cm -1
(CO)= 1829, 2019, 2082 cm -1
Three bond modes found in metal carbonyl compounds
The terminal mode is the most frequently one mode found exhibiting a carbon oxygen triple bond i.e., Ni(CO)4
The double or triply-bridged mode is found in many polynuclear metals carbonyl compounds with an electron deficiency i.e., Rh6(CO)16 (four triply bridged CO groups)
Which modes are present in a given compound can often be determined by infrared and 13C-NMR spectroscopy
Structures I
M
C
O
M M
C
O
M
M
M
C
O
terminal 2 3
Mononuclear compounds
Dinuclear compounds
Structures II
M
OC
OC CO
CO
CO
CO
OC M
CO
CO
CO
CO
CO
M
OCCO
CO
M(CO)6 (Oh) M(CO)5 (D3h) M(CO)4 (Td) i.e., Cr(CO)6 i.e., Fe(CO)5 i.e., Ni(CO)4
CO
M
CO
OCOC
OC
M
COOC
COOC
CO
OC
Fe
OC
OC
OC CO
Fe
COOC
CO
CO
OC
Co
OC
OC
OC
Co
COOC
CO
CO
Co
CO
OC
OC
OC
Co
CO
COOC
CO
M2(CO)10 (D4d) Fe2(CO)9 (D3h)i.e., Re2(CO)10
Co2(CO)8 Co2(CO)8
(solid state, C2v) (solution, D3d)
Free CO: 2143 cm-1
Terminal CO groups: 1850-2125 cm-1
m2-brigding CO groups: 1750-1850 cm-1
m3-bridging CO groups: 1620-1730 cm-1
Non-classical metal carbonyl compounds can have n(CO) greater than the one observed in free CO
Infrared Spectroscopy
Compound n(CO) [cm-1] d(CO) [pm]
Ni(CO)4 2057 112.6
Fe(CO)5 2013, 2034 112.2, 114.6
Cr(CO)6 2000 114.0
Re2(CO)10 1976, 2014, 2070 112-113, 114.7
Fe2(CO)9 1829, 2019, 2082 112.6, 116.0
Rh6(CO)16 1800, 2026, 2073 115.5, 120.1
Ag(CO)2+ 2185 108.0
Terminal CO: 180-220 ppmBridging CO: 230-280 ppmExamples:
M(CO)6: Cr: 211 ppm, Mo: 201.2 ppm, W: 193.1 ppmFe(CO)5
Solid state: 208.1 ppm (equatorial) and 216 ppm (axial) in a 3:2-ratio Solution: 211.6 ppm (due to rapid axial-equatorial exchange)
Fe2(CO)9 (solid state): 204.2 ppm (terminal), 236.4 ppm (bridging)
Co2(CO)8 Solid state: 182 ppm (terminal), 234 ppm (bridging)Solution: 205.3 ppm
13C-NMR Spectroscopy
Collman’s reagent This reagent is obtained from iron pentacarbonyl and sodium hydroxide in
an ether i.e., 1,4-dioxane It exploits the labile character of the Fe-C bond of alkyl iron compounds
which allows for the insertion of a CO ligand, which technically generates a “RC=O-”.
Advantages: high degree of chemoselectivity, produces high yields (70-90 %), bears low cost and is relatively environmental friendly
Application I
+ 2 NaOH Na2Fe(CO)4 Collman's ReagentFe(CO)5
RX
RFe(CO)4-
R'X
R R'
O
O2
RCOOH
X2
RCOX
RCOCl
(RCO)Fe(CO)4-
D+
R-D
H+
RCHO
Fischer Tropsch Reaction/ProcessThe reaction was discovered in 1923The reaction employs hydrogen, carbon monoxide and
a “metal carbonyl catalyst” to form alkanes, alcohols, etc.Ruhrchemie A.G. (1936)
Used this process to convert synthesis gas into gasoline using a catalyst Co/ThO2/MgO/Silica gel at 170-200 oC at 1 atm
The yield of gasoline was only ~50 % while about 25 % diesel oil and 25 % waxes were formed (How many candles do you need today? )
An improved process (Sasol) using iron oxides as catalyst, 320-340 oC and 25 atm pressure affords 70 % gasoline
Application II
Second generation catalyst are homogeneous i.e., [Rh6(CO)34]2-
Union Carbide: ethylene glycol (antifreeze) is obtain at high pressures (3000 atm, 250 oC)
Production of long-chain alkanes is favored at a temperature around 220 oC and pressures of 1-30 atm
Application III
MCO
M COH2 M C H
OH2
M CH3CO
M COCH3
MCH2
O
H2
H2
M OCH3
M H
CH3OH
H2 H2
M CH3
H
CH4
M
M CH2 CH3
CO
M COCH2CH3
Gasolines
Monsanto Process (Acetic Acid)This process uses cis-[(CO)2RhI2]- as catalyst to convert methanol
and carbon dioxide to acetic acidThe reaction is carried out at 180 oC and 30 atm pressure
Two separate cycles that are combined with each other
Application IV
CH3OH
HI H2O
CH3COOH
CH3I
Rh
COI
I CO
Rh
COI
I CO
CH3
I
Rh
COCH3I
I CO
I
Rh
COCH3I CO
COI
CO
CH3COI
I
Oxidative Addition(+I to +III)
Reductive Elimination(+III to +I)
CO Insertion
CO Addition
Hydroformylation It uses cobalt catalyst to convert an alkene, carbon monoxide and
hydrogen has into an aldehyde The reaction is carried at moderate temperatures (90-150 oC) and high
pressures (100-400 atm)
Application V
HCo(CO)4
HCo(CO)3
CO
CH2=CHR
HCo(CO)3(CH2=CHR)
RCH2CH2Co(CO)3
RCH2CH2Co(CO)4 CO
RCH2CH2COCo(CO)3
RCH2CH2COCo(H2)(CO)3
H2
RCH2CH2CHO
The Pauson–Khand reaction is a [2+2+1] cycloaddition reaction between an alkene, alkyne and carbon monoxide to form an α,β-cyclopentenone.
Originally it was catalyzed by dicobalt octacarbonyl, more recently also by Rh-complexes (i.e., Wilkinson’s complex with silver triflate as co-catalyst)
Application VI
R'
R'
R
R R
R
+ CO+Co2(CO)8
O
R
R
R
R
R'
R'
Reppe-CarbonylationAcetylene, carbon monoxide and alcohols are reacted in
the presence of a catalyst like Ni(CO)4, HCo(CO)4 or Fe(CO)5 to yield acrylic acid esters
If water is used instead of alcohols, the carboxylic acid is obtained (i.e., acrylic acid)
The synthesis of ibuprofen uses a palladium catalyst on the last step to convert the secondary alcohol into a carboxylic acid
Application VII
(CH3CO)2O/HF
O
H2, Raney Ni
OH
CO, [Pd]
COOH
Doetz reactionCarbonyl compounds are
reactant to form metal- carbene complexes (Fischer carbenes)
The addition of an alkyne leads to the formation of a metallacycle
Next, one of the carbonyl groups is inserted into the Cr-C bond
The electrophilic addition of the carbonyl function to the phenyl group affords a naphthalene ring
Application VIII
Cr(CO)6
1.PhLi2.MeI
(CO)5Cr
Ph
OMeR-C C-R
(OC)5Cr Ph
OMe
RR
(OC)5Cr
Ph
OMe
R
R
CO insertion
Ph
OMe
RR
OC
(OC)4CrOMeC
R
O
RCr(CO)4
H
O
R
R
OMe(OC)4Cr
OH
R
R
OMe(OC)3Cr
OH
R
R
OMe
Cr(CO)3
+
1. Loss of CO2. Enolization