data-driven discovery and optimisation of organometallic...
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Data-driven discovery and optimisation of organometallic catalystsDr Natalie Fey
Dial-a-Molecule Annual Meeting
3rd July 2019, York
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Opportunities from Data
▪ Select “best” synthetic route– Better use of resources/time.
– Break “cultural attachments” to routes.
– Find new approaches.
– When to stop.
▪ Broaden our toolkit, explore new chemistry.
▪ Deepen our understanding (mechanism, catalyst/substrate matching).
▪ Combine experiment and computation to work towards prediction.
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Chem. Central J. 2015, 9, 38
Property Databases
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Ligand Knowledge Bases▪ Ligands used to tune complex
properties.
▪ Characterise ligands (size, electronics).
▪ Map ligand properties.
▪ Derive structure-property relationships.
▪ Are two dimensions sufficient?
▪ Transferability to other ligand types.
80 100 120 140 160 180 200
Cone Angle (°)
2060
2080
2100
TE
P (
cm
-1)
CHCH2
R
Ar
Hal
OR
NR2
PF3
PCl3
P(C6F
5)3
P(O-o-tBu-C6H
4)3
P(o-tolyl)3
PtBu3PCy
3
PiPr3
P(NMe2)3
PBz3
PPh3
PEt3
PMe3
PH3
P(OEt)3
P(OMe)3
P(OPh)3
electron
withdrawing
electron
donating
small large
Tolman, Chem. Rev. 1977, 77, 313–348.
For other examples: QALE, Cundari, Rothenberg.
See Coord. Chem. Rev. 2009, 253, 704-722.
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LKB-P▪ 28 descriptors, quite highly correlated.
▪ Projection methods:– Reduce number of variables (dimensions) by transformation of original
variables.
– Optimally represent distances between objects.
▪ Principal Component Analysis– Describe variation of data in terms of uncorrelated variables.
– Derive from linear combinations of original variables.
– Maximum variance in first PC, decreasing order of importance, orthogonal.
PC1 = a1,11 + a1,22 + … + a1,nn
PC2 = a2,12 + a2,22 + … + a2,nn
BP86/6-31G*, LACV3P on Au, Pd, Pt
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PA3, PA2B, A =RCH2=CH2
SiMe3
ArOR/OArNR2/NAr2
HalPABC
PI3
PBr3
PCl3
PF3
PtBu3
PMe3
P(CF3)3
PMe2(CF3)
PMe(CF3)2
P(C6F5)3
PPh3
P(OMe)3
P(OPh)3
Organometallics, 2010, 29, 6245;
Chem. Eur. J. 2006, 12, 291Dr Jesús Jover, with JNH, AGO, GCLJ
28 descriptors, 348 L, 65%
LKB-P Map
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Other ligands
LKB-PP
Organometallics, 2012, 31, 5302;
Organometallics 2008, 27, 1372
LKB-PPscreen
Dalton Trans. 2013, 42, 172
(i) Me
(ii) CF3
(iii) tBu
(iv) Ph
(v) C6F5
(vi) o-tol
(vii) p-tol
(viii) p-CF3-Ph
(ix) OMe
(x) OPh
(xi) NMe2
A2P~PA2, A=N
EW
S
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Other ligands
LKB-PP
Organometallics, 2012, 31, 5302;
Organometallics 2008, 27, 1372
LKB-PPscreen
Dalton Trans. 2013, 42, 172
LKB-C
Dalton Trans. 2009, 8183
(i) Me
(ii) CF3
(iii) tBu
(iv) Ph
(v) C6F5
(vi) o-tol
(vii) p-tol
(viii) p-CF3-Ph
(ix) OMe
(x) OPh
(xi) NMe2
A2P~PA2, A=N
EW
S
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Bidentate Ligand Space
with Dr Charlotte Willans, Dr Bao Nguyen, Prof. Andrei
Malkov, Dr Jonathan Moseley, Dr Simon Tyler
224 ligands, 52%
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C-, N-, O-donor ligands only
146 ligands, 57%
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Publication in preparation
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Dr Gareth Owen-Smith, Dr Jesús Jover, with
Jeremy Harvey, Guy Orpen, Guy Lloyd-Jones
Experiment
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Dr Gareth Owen-Smith, Dr Jesús Jover, with
Jeremy Harvey, Guy Orpen, Guy Lloyd-Jones
Experiment
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Global Models:
-15 -10 -5 0 5
PC1
-11
-6
-1
4
PC
2
LM5: Q(B fragm.), Q(Pd fragm.), Q(Pt
fragm.), BE(Au), BE(Pd), P-Pt, P-A(B),
P-A(Pt) [8], R2 = 0.687, CV PE = 0.83
-4.00
-3.00
-2.00
-1.00
0.00
1.00
2.00
3.00
-8.00 -6.00 -4.00 -2.00 0.00
LM
5 R
es
idu
als
LM5 Predicted log(initial rate)
Dr Gareth Owen-Smith, Dr Jesús Jover, with
Jeremy Harvey, Guy Orpen, Guy Lloyd-Jones
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LASSO (1000 random samples)
Dr Ben Swallow (JGI Seedcorn Funding)
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Beyond Ligands…
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Alkynes & Vinylidenes
with Dr Jason Lynam,
Organometallics, 2014, 33, 1751
Tautomer Preference Ev-a(Ru)
Chem. Commun. 2015, 51, 9702
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64 pairs, 56 %
with Prof. Paula Diaconescu
Redox-Switchable Catalysts
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64 pairs, 56 %
Chem. Commun., 2019, 55, 7021-7024
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MechanismM
M
A
A
B
M
A
B
M
AB
AB
M
A
B1
B2
AB1 M
B2
+
Unwanted
Desired
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Bristol Reactivity in Catalysis Knowledgebase (BRiCK)
▪ Target: New applications for known catalysts.
▪ Systematic study of catalytic cycles.– Phase 1: Substrate effects on barriers.
– Phase 2: Catalysts modification (metal, ligands).
– Phase 3: Test experimentally.
– Repeat…
Derek Durand, with Prof. Paul Pringle, Dr Jason Lynam,
Dr Ruth Webster, Dr Alex Cresswell,
coming soon: Dr Thibault Cantat, Dr Jordi Carbo
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Derek Durand
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Jaguar 8.5, B3PW91-D3, 6-31G(d), 298 K, PCM (methanol)Derek Durand
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Substrate (U) ∆∆G Oxidative Addition (kcal mol-1)Ethene 9.23Acetylene 4.90Carbon Monoxide 8.71
Substrate (U) ∆∆G Reductive Elimination (kcal mol-1)Ethene 5.29Acetylene 5.12
Carbon Monoxide 3.93 Derek Durand
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Conclusions▪ Databases of descriptors (ligands, substrates, catalysts).
– Maps.
– Models (experimental and computational responses).
– Screening – design and optimisation.
▪ Mechanism.– Reasonable accuracy.
– Multiple catalysts.
– Selectivity and change in mechanism remain challenging.
▪ Now moving on to mapping reactivity – BRiCK, with experimental testing.
▪ Extreme value prediction.
We like data!
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Acknowledgements▪ Derek Durand, Claire McMullin, Jesús
Jover, Gareth Owen-Smith, Ben Swallow, Mairi Haddow, Keshan Bolaky, Ben Rawe, Tim King
▪ Paul Pringle, Jeremy Harvey, Guy Orpen, Guy Lloyd-Jones
▪ Jason Lynam, Charlotte Willans, Bao Nguyen, Andrei Malkov, Jonathan Moseley, Simon Tyler, Paula Diaconescu, Ruth Webster, Alex Cresswell
▪ Bristol Centre for Computational Chemistry
(CLM)
(JJM)
University of York pump-priming fund, JGI Seedcorn Funding
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bris.ac.uk/chemistry/facilities/basf
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Physical Insights into Mechanistic Processes in Organometallic Chemistry
Faraday Discussion
2– 4 September 2019York, UK http://rsc.li/organometallic-fd2019
Upcoming deadlines
Early bird registration – 15 July 2019
Standard registration – 05 August 2019