Phosphorus Ligand Effects in Homogeneous Catalysis ... - Wiley
Organometallic Chemistry for Homogeneous Catalysis
Transcript of Organometallic Chemistry for Homogeneous Catalysis
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David Cole-Hamilton
EaStCHEM,
University of St. Andrews
President EuCheMS
Organometallic Chemistry for
Homogeneous Catalysis
Dedicated to all who suffer as a result of the Italian
earthquakes, especially in Camerino
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Thanks to:
Paul Kamer
University of St Andrews
Bob Tooze
Sasol Technology UK Ltd (St. Andrews)
Piet van Leeuwen
University of Amsterdam, ICIQ Tarragona
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Books
Homogeneous Catalysis: Understanding the Art
Piet W. N. M van Leeuwen, Kluwer Dordrecht,
2004
Applied Homogenous Catalysis with Organometallic
Compounds,
Eds. B. Cornils and W. A. Herrmann, Wiley, VCH,
Weinheim, 2002
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Outline
• Background to Catalysis
• Basic Principles of Homogeneous Catalysis
• Selected Examples
• Using Bioresources
• Catalysts Separation and recycling
• Flow homogeneous catalysis
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Energy profile of a reaction
A catalyst lowers the activation
energy of a reaction
No catalyst
Catalyst
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How Does a Catalyst Work?
•Lowering activation energy
•Stabilization of a reactive transition state
•Bringing reactants together
•proximity effect
•orientation effect
•Enabling otherwise inaccessible reaction paths
触媒 Tsoo Mei
Marriage broker - catalyst
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P Prevent waste
R Renewable materials
O Omit derivatisation
D Degradable chemical products
U Use safe synthetic methods
C Catalytic reagents
T Temperature, pressure ambient
I In-process monitoring
V Very few auxiliary substances
E E-factor, maximise feed in product
L Low toxicity of chemical products
Y Yes, it is safe
12 Principles of Green Chemistry
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√
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√
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√
P. Anastas J. Warner
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E Factor
E-Factor = total waste (kg) / product (kg)
Industry
segment
Product tonnage E-Factor
Oil refining
Bulk chemicals
Fine chemicals
Pharmaceuticals
106-108
104-106
102-104
10-103
<0.1
<1-5
5-50
25-100
E-Factors in the chemical industry
E-Factor in Pharmaceuticals:
Multiple step syntheses
Use of classical stoichiometric reagents
However, lower absolute amount (compared to bulk).
R. Sheldon
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Advantages of Catalytic Process
New catalytic process water is only waste
Methyl Methacrylate (for Perspex)
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Different types of Catalyts
Heterogeneous • Usually a solid in a different phase from the reactants
• Usually metal or metal oxide
Homogeneous • In the same phase as the reactants
• Usually a dissolved metal complex
Enzyme (Biological) • Usually a complex system in water
• Highly active and selective
• Sometimes rather unstable
• Becoming increasingly popular
World Catalyts market $ 9 billion
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Heterogeneous vs Homogeneous Catalysis
Heterogeneous Homogeneous
Solid metal or metal oxide Metal complex
Solvent not required Solvent required (usually)
Thermally robust Thermally sensitive
Only surface atoms available All metal centres available
Selectivity can be poor Selectivity can be tuned
Difficult to study while operating In situ spectroscopy
Easy separation from products Difficult product separation
Some processes only
heterogeneous
N2 + 3 H2 2 NH3
Exhaust catalyst
Some processes only
homogeneous
MeOH + CO MeCO2H
Hydroformylation of alkenes
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Selectivity / Hydroformylation
Chemoselectivity
Regioselectivity
Enantioselectivity
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Counting electrons
• Determine the oxidation state of the metal and hence
the number of d electrons.
• Add 2 for each ligand (note that benzene coordinates
through the 3 double bonds so gives 6).
• Add electrons for overall negative charges, subtract
electrons for overall positive charges.
RhIII 4d6 6 e
6 x 2e ligands 12 e
Total 18 e
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Reactions in catalytic cycles
• Need a vacant site (often 14 or 16 e intermediate)
RhIII 4d6 6 e
5 2e ligands 10 e
Total 16 e 18 e
Coordination
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Bonding of alkenes
• Donation of electron density from p orbital on
C=C to an empty s, p or d orbital on the metal
• Back donation of electron density from the filled
t2g level on the metal to the empty p* orbital on C=C
Adds 2 e
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Bonding of CO
.
• Donation of a lone pair of electrons from the C
atom of CO to an empty s, p or d orbital on the
metal
• Back donation of electron density from the filled
t2g level to the empty p* orbital on CO
Adds 2 e
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Substitution
Octahedral complexes
Mechanism
[ML6]n+ + L’ → [ML5L’]n+ + L
1) Dissociative (SN1)
0 order in L1. DS‡ will be positive
2) Associative (SN2)
[ML6]n+ + L’ → [ML6L’]n+ → [ML5L’]n+ + L
7 coordinate
1st order in L’ DS‡ negative
3) Hybrid mechanisms No change in e count
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Oxidative Addition
Concerted addition
[RhCl(PPh3)3] + H2
Kubas, G. J.; Ryan, R. R.; Swanson, B. I.; Vergamini, P. J.; Wasserman,
H. J., J. Am. Chem. Soc., 1984, 106, 451
RhI 16 e RhIII 18 e
Adds 2 e
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Alkyl halides – Sn2
Should give inversion of configuration
J. K. Stille and K. S. Y. Lau, Acc. Chem. Res. 1977, 10, 434
If both pathways have similar energy partial racemisation will occur
Trans addition usually goes
by this mechanism
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s-bond metathesis
Occurs when metal is in highest oxidation state (d0) and oxidative
addition is not possible
No change in e count
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Migratory insertion
• Incoming ligand does not insert
• Incoming ligand ends up cis to the acyl
• Me and CO involved in migration are mutually cis
Which moves?
Me must move. If CO moves cannot get C
A B C
Retention of configuration
Removes 2 e
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Hydride migration and b-hydrogen abstraction
Alkene isomerisation
Adds 2 e
Removes 2 e
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Takasago Menthol Synthesis
Cat =
[RhI(BINAP)2]+ClO4
-
TON = 400.000
K. Tani, T. Yamagata, S. Akutagawa, H. Kumobayashi, T. Taketomi, H. Takaya. A.
Miyashita, R. Noyori and S. Otsuka, J. Am. Chem. Soc., 1984, 106, 5208
Planar
chirality
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Attack on Coordinated ligands
Nucleophilic Electrophilic
E. O. Fischer and co-workers No change in e count
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The Wacker Process
[PdCl4]2- + C2H4 + H2O → CH3CHO + Pd + 4 Cl- + 2 H+
Pd + 2 Cu2+ + 4Cl- → [PdCl4]2- + 2 Cu+
2 Cu+ + ½ O2 + 2 H+ → Cu2+ + H2O
C2H4 + ½ O2 → CH3CHO
1970’s 2 M tonnes per year - decreasing
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Mechanism
Step B:
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Unit steps in Catalytic reactions
Introduction of substrates onto metal centre
- Simple Coordination
- Substitution
- Oxidative Addition
- Sigma bond metathesis
Reactions between substrates in coordination sphere.
- Migratory insertion
- Attack of Nucleophiles onto coordinated ligands
- b-H abstraction
Releasing substrates from Metal Centre.
- Decoordination
- Substitution
- Reductive Elimination
- Sigma bond metathesis
Reverse of introduction
Change in No
of electrons
+2
0
+2
0
-2
0
+2
-2
0
-2
0
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16/18 e Rule
• Catalytic cycles often proceed through a variety of intermediates
alternating between 16 and 18 electrons
RhI, 16 e
RhIII, 18 e
RhIII, 16 e RhIII, 18 e
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Register now!
A Gordon-style conference for chemists around
the Atlantic Basin
23-26 January, 2018
Register NOW at http://abcchem.org/registration/
http://www.rsc.org/events/euchems2018
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Catalytic hydrogenation (Wilkinson’s catalyst)
By 31P and 1H NMR spectroscopy see only compound 2 , a resting state
outside the catalytic cycle – no information about cycle
Kinetics suggest H migration onto alkene is rate determining
Parahydrogen allows detection of II
Duckett et al, J. Am. Chem. Soc, 1994, 116, 10548
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Asymmetric hydrogenation
W.S. Knowles and M.J. Sabacky, Chem. Commun., 1968, 481
W. S. Knowles
Nobel Prize, 2001
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Ketone hydrogenation
Rhodium based catalysts are usually of very low activity unless very electron rich (e. g. [RhH(CO)(PEt3)3] for aldehyde hydrogenation, J. K. MacDougall et al, J.
Chem Soc. Dalton Trans., 1996, 1161)
Ruthenium based catalysts are preferred
Asymmetric Catalysis by Architectural and Functional Molecular Engineering:
Practical Chemo and Enantioselective Synthesis of Ketones
R. Noyori and T. Ohkuma Angew..Chem.Int. Edi. 2001,40, 40-73.
R. Noyori
Nobel Prize, 2001
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Hydrogenation of activated ketones
R. Noyori and T. Ohkuma Angew..Chem.Int. Edi. 2001,40, 40-73.
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Ligands for asymmetric ketone hydrogenation
R. Noyori and T. Ohkuma Angew..Chem.Int. Edi. 2001,40, 40-73.
Non-classical
ligands
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Outer sphere mechanism
P. A. Dub and J. C. Gordon, Dalton Trans., 2016,45, 6756
Addition of H+
and H-
Substrate does
not bind to the
metal
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Hydroformylation
100 % atom economy
Liquid and gaseous substrates
Issues of Selectivity
Problems with product separation
Industrially very important
C4 6 M Tonnes y-1
C9 – C14 1.5 M tonnes y-1
Plasticisers, soaps, detergents
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Butanal
High linear selectivity is essential
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Hydroformylation mechanism
RCH(Me)CHO
branched
linear
Coordination
H migration
Coordination
migration
Oxidative addition
Reductive
elimination
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Linear branched selectivity
For high linear selectivity – need
• excess of large ligands e. g. PPh3 Rh:P = 30:1, l:b = 15
• Low pCO
• OR bidentate ligand with a bite angle near 120o
2 P equatorial (ee) – angle is 120o
1 P equatorial, 1 axial – angle is 90 o
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Structure-selectivity relation
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Carbonylation of methanol (Cativa)
A. Haynes, P. M. Maitlis, G. E. Morris, G. J. Sunley, et alJ. Am. Chem. Soc.,
2004, 126, 2847-2861.
Fast for Rh
Slow for Ir
Anionic
Ox Addn fast
Migration v slow
Neutral
Ox addn slow
Migration fast
Need to cycle
Between two
Acetic acid 16 M tonnes pa
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Ethene carbonylation (Lucite)
120,000 tonnes per year
Singapore
TOF = 12,000 h-1 TON = > 1,000,000 Selectivity = 99.9 %
D. Johnson, http://www.soci.org/chemistry-and-industry/cni-data/2009/20/a-winning-process
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Methoxycarbonylation of alkenes
[Pd2(dba)3] (0.05 mmol)
CH3SO3H (1 mmol), alkene (12.7 mmol), methanol (10 cm3),
CO (1-4 bar) 20 oC, 3 h
(0.5 mmol)
C. Jiménez Rodriguez, D. F. Foster, G. R. Eastham, and D. J. Cole-Hamilton,
Chem. Commun., 2004, 1720-1721
97 % terminal
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Isomerisingmethoxycarbonylation
of unsaturated esters Conv Sel
% %
100 96.3
100 99
100 97.3
17.3 100 1 bar, 20 oC
30 bar 80 oC
C. Jiménez Rodriguez, G. R. Eastham and D. J. Cole-Hamilton, Inorg. Chem.
Commun., 2005, 8, 878.
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Buchwald-Hartwig amination
Suzuki
Cross coupling reactions: a success story
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Heck Coupling Mechanism
Blackmond and coworkers, Angew Chem. Int. Ed. 2005, 44, 4302; J. Am.
Chem. Soc., 2001, 123, 1848
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metathesis: from Greek
meta, change; tithenai, place Cross-Metathesis
Alkene Metathesis
+ 2
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Well-Defined Metathesis Catalysts
Grubbs “2nd
generation” Ru
PCy3
Cl
Cl
Cy3PC
H
RuCl
Cl
Cy3PC
H
N
N
OO
Mo
R''
R''
N
R R
R'
Schrock Range of biphen / binaphtholates
tunable: ARCM, chiral ROMP
Grubbs I Robust (>> tolerant of air, water, polar functional-groups)
Very wide range of processes catalyzed by Ru
Nobel Prize, 2005 with Yves Chauvin
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Ethene polymerisation
Cp2ZrMe2 + MAO [Cp2ZrMe]+
partially hydrolysed Me3Al
W. Kaminsky, K. Kulper, H. H. Brintzinger and F. Wild,
Angew. Chem.-Int. Edit. Engl., 1985, 24, 507
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Oil - What next?
Fuels
Chemicals ?
Demand is too high
Land use, fuel vs food
Contribution
10 % biodiesel in UK
diesel
?
Using waste streams are best
4 %
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Waste Oils
300,000 tonnes per year
Cashew nut shell liquid (food)
Kraft
Process
NaOH / Na2S
2 M tonnes per year
Tall Oil (paper)
85 %
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Uses of a,w-difunctionalised
compounds
Fibres Elastomers
Thermoplastics Melt adhesives
Coatings Engineering plastics,
Nylons (2 M tonnes per year).
Overall 3 M tonnes per year
Polyethylene replacement (biodegradeable)
Polyamide (nylon)
D. Quinzler and S. Mecking, Angew Chem. 2010, 49, 4306; F. Stempfle, D. Quinzler, I. Heckler, S.
Mecking, Macromolecules 2011, 44, 4159-4166
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Biodegradable
Desirable Undesirable
Manila Harbour
Oilprice.com
Gas pipeline
(HDPE 50 % of all polyethylene)
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Oleochemicals
C. Jimenez-Rodriguez, G. R. Eastham and D. J. Cole-Hamilton, Inorg. Chem. Commun., 2005, 8, 878.
[Pd] = 0.008 mol dm-3, [DTBPMB] = 0.04 mol dm-3, [MSA] = 0.08 mol dm-3, substrate (2 cm3, 6 mmol),
methanol (10 cm3), pCO = 30 bar, 80 °C, 22 h,
CO + MeOH
Methyl ester Yield (sat diester)/% linear selectivity / % Other prods (%)
oleate 95 > 95 25 g
High oleic sunflower oil – 3.5 kg in 12 dm3 autoclave
G. Walther, J. Deutsch, A. Martin, F.-E. Baumann, D. Fridag and A. Köckritz,
ChemSusChem, 2011, 4, 1052
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Methoxycarbonylation of natural oils
Methyl oleate
(Aldrich)
Olive
(Tesco)
Rapeseed
(Tesco)
Sunflower
(Tesco)
Oleate / % >90 73 64 38
Linoleate / % 2 19 50
Linolenate / % 3 10 2
Diester / g from
10 mL oil
9.0 6.9 6.4 3.4
Yield / %
(from oleate)
74.7
102.3
69.3
108.3
36.8
96.8
Cost of diester
/ kg-1
$ 6500 (>99
%)
$ 50 (70 %)
$ 4.3 $ 1.3
Marc Furst
M. R. L. Furst, R. le Goff, D. Quinzler, S. Mecking and D. J. Cole-Hamilton, Green. Chem. 2012, 14, 472
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Tall Oil Fatty Acids (TOFA)
Marc Furst
28 % 72 %
Presterified and dried
Isolated 49 %
M. R. L. Furst, T. Seidensticker and D. J. Cole-Hamilton, Green Chem., 2013, 15, 1218
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Why so selective?
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Catalyst recovery and recycling
D. J. Cole-Hamilton, Science, 2003, 299, 1702
D. J. Cole-Hamilton and R. P. Tooze, eds.,
Catalyst Separation, Recovery and Recycling; Chemistry and Process
Design, Springer, Dordrecht, 2006
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Hydroformylation Conditions
Parameter Cobalt /(+phosphine)
Temperature / o C
Pressure / bar
l:b
Side reactions
120-160 (150-190)*
270-300 (40-100)
3:1 (10:1)
(Alkanes, alcohols , esters, acetals)
Rhodium / PPh3
80-120
12-25
12:1
Condensed aldehydes (used as solvent)
Stability
Catalyst recovery
Stable to high T
Difficult but possible
Decomposes at 110 oC
Easy <C7
* Rate is reduced by a factor of 4-6
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Problems with Homogeneous Catalysts
• - Separation of the solvent, catalysts and product
• - Recycling of the catalyst
• - The use of volatile organic solvents
• - Batch or batch continuous processing
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The separation problem
Now please bring me:
• The pure coffee
• The pure sugar
• The pure milk
• The pure water
All from this cup of coffee
All with 100 % recovery
Please make me
a cup of coffee
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Originally proposed by J. Manessan in Progress in Research, Eds F. Basolo
and R. L. Burwell, Plenum Press, London, 1973, p 183
Originally demonstrated by E. Kuntz, Fr. Demande, 1975, 2,314,910
Aqueous biphasic catalysis
Substrate
H2O
Product
Catalyst
Gases
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Vent
Propene
CO/H2
Str
ipp
er
Dis
tilla
tion
Re
acto
rDecanter
iso-
n-
1
2
3
4
5
6
Ruhrchemie Reactor
Only operational for propene
Low solubility of higher alkenes
limits mass transfer
< 1 ppb Rh loss
E. Wiebus and B. Cornils in Catalyst separation, recovery and recycling: Chemistry and
process Design, Eds D. J. Cole-Hamilton and R. P. Tooze, Springer, Dordrecht, 2006, p 105
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Continuous flow reactor for low volatility
substrates and products
Substrates
in scCO2
Products
in scCO2
Liquid catalyst
or
Catalyst in involatile solvent Solvent
• - Involatile
• - Insoluble in scCO2
• - Dissolves catalyst
Catalyst
• - Soluble in solvent
• - Insoluble in scCO2
IONIC LIQUID? IONIC CATALYST
P. B. Webb, M. F. Sellin, T. E. Kunene, S. Williamson, A. M. Z. Slawin and D. J
Cole-Hamilton, J. Am. Chem. Soc., 2003, 125, 15577
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Flow homogeneous catalysis
D. J. Cole-Hamilton, Science, 2003, 299, 1702-1706
IL
P
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SILP hydroformylation with SCF flow
+ CO + H2
CHO
CHO
+
scCO2
scCO2
Rh-P
Rh-P
IL
IL
N NPh2P
SO3-
+
N N+
[N(SO2F)2]-
IL
P
U. Hintermair, Z. Gong, A. Serbanovic, M. J. Muldoon, C. C. Santini and
D. J. Cole-Hamilton, Dalton Trans, 2010, 39, 8501
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Catalyst stability
0
2000
4000
6000
8000
10000
12000
14000
16000
18000
20000
0.0 5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0
Time / h
Cata
lyst
turn
overs
TOF = 500 per h
U. Hintermair, G. Y. Zhao, C. C. Santini, M. J. Muldoon, and D. J. Cole-Hamilton
Chem. Commun., 2007, 1462
< 0.5 ppm Rh
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It does, for example, no good to offer an elegant, difficult and expensive process to an industrial manufacturing chemist, whose ideal is something to be carried out in a disused bathtub by a one-armed man who cannot read, the product being collected continuously through the drain hole in 100% purity and yield.
What we really want
Sir John Cornforth, Chemistry in Britain, 1975, 342.
Continuous FLOW
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Bath or Shower?
+ H2
cata
lyst
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Solventless reaction Ruben Duque
22 ºC, H2 (5 bar, 0.2 dm3 min-1), substrate ( neat, 0.05 ml min-1) 9580 TON after 80.5 h, 400 g week-1
R.L. Augustine∗, S.K. Tanielyan, N. Mahata, Y. Gao, A. Zsigmond, H. Yang, Applied Catalysis A: General 2003, 256, 69–76
0
20
40
60
80
100
0 20 40 60 80
%
time (h)
conversion e.e.
Rh 44-625 ppb
Pure single
enantiomer 1
R. Duque, P. J. Pogorzelec and D. J. Cole-Hamilton, Angew. Chem., Int. Ed., 2013, 52, 9805
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Conclusions
Homogeneous Catalysts
ROCK