Muon Spectroscopy of Molecules · 2017. 5. 15. · Agrees with NMR & QENS values. Photoelectron...
Transcript of Muon Spectroscopy of Molecules · 2017. 5. 15. · Agrees with NMR & QENS values. Photoelectron...
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MuonMuon Spectroscopy of MoleculesSpectroscopy of Molecules
Upali Upali A. A. JayasooriyaJayasooriya
School of Chemical Sciences and PharmacySchool of Chemical Sciences and Pharmacy
University of East University of East AngliaAnglia
NorwichNorwich
UKUK
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IntroductionIntroduction
• Muon Muon states in matterstates in matter
Implanted positiveImplanted positive muonsmuons may exist in any of the may exist in any of the following forms.following forms.
a) a) MuonMuon µµ++
b) b) MuoniumMuonium µµ++ee--
c) Part of a radicalc) Part of a radical
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µµSRSR•• Properties of Properties of MuonsMuons??
Mass = 0.11 protonMass = 0.11 proton
Charge = +eCharge = +e
Spin = 1/2Spin = 1/2
Magnetic moment = 3.18 x protonMagnetic moment = 3.18 x proton
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µµSRSR
•• Properties of Properties of MuoniumMuonium [[µµ++ee--]]
Isotope Mass/me Reduced mass/me Bohr radius/nm Ionisation energy/eV
Tritium (3H) 5498 0.9998 0.05290 13.603
Deuterium (2H) 3675 0.9997 0.05293 13.602
Protium (1H) 1847 0.9995 0.05292 13.599
Muonium (Mu) 208 0.9952 0.05315 13.541
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µµSRSR
•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
Some of the names to look out for
•Paul Percival•Emil Roduner•David Walker•Donald G. Fleming•Christopher Rhodes•Brian Webster•Rod Macrae
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µµSRSR
•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]Chemiluminescence from the
exiplex molecule NeMu*
S. Baer et. al. J. Chem. Phys. 101 (1994) 1202
Dissociative state, Ne + Mu
Exciplex, NeMu*
Ne-Mu distance
Molecular potential energy
Prompt
Delayed
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Muon - Electron system; Breit - Rabi diagram
Singlet
Energy
Magnetic FieldTriplet
Aµ
e- µ+
⌧3>
⌧2>
⌧4>
⌧1>
ms
+1
0
-10
Pashen-Back regime
H = hAµ S.I + hωeSz + hωµIz
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Muon - Electron system; Breit - Rabi diagram
Singlet
Energy
Magnetic Field
Triplet
Aµ ν24
ν12
ν34
e- µ+
+ +
+ -
- -
- +
⌧3>
⌧2>
⌧4>
⌧1>
ms
+1
0
-1
0
Polarisation
Relaxation
LF
-time differential
Rotation
TF
ALC
LF
-time integral
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µµSRSR
•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
carbonyl groups:carbonyl groups: C = OC = OEn
ergy
σ
nπ
σ∗
π∗ LUMO
Mu
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TF-MuSR spectra of
(a) 4-Fluoroacetophenone,
(b) 4-Chloroacetophenone
& (c) 4-Methylacetophenone
at 200 mT and 300 K
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µµSRSR
•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
Mu.
Mu.
EtheneCH2 = CH2
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DNA
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µµSRSR
•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
4
5N7
N9 N3
2
N16
8
NH26
R
4
5N7
N9 N3
2
NH16
8
R
O
NH22
6
5
N1
2
NH34
O4
O2
R
CH3
6
5
N1
2
NH34
O4
O2
R
URACIL THYMINE CYTOSINE
GUANINE ADENINE
6
5
N 1
2
N34
NH24
O2
R
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µµSRSR•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
1.4 1.6 1.8 2.0 2.2 2.4 2.6
-0.4
-0.3
-0.2
-0.1
0.0
0.1
0.2
0.3
0.4
Field / T
Derivative of polarisation
300K
Adenine
100K
1.3 1.4 1.5 1.6 1.7 1.8 1.9 2.0 2.1 2.2
1.4
1.6
1.8
2.0
2.2
2.4 Guanine; C5
Cytosine; C6
Adenine; C2
Uracil; C6
Thymine; C5
Adenine; C8
Guanine; C8
Experimental field / T
Theoretical field / T
ALC |∆M| = 1 resonance features
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µµSRSR•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
1.4 1.6 1.8 2.0 2.2 2.4 2.6 2.8 3.0 3.2
1.4
1.6
1.8
2.0
2.2
2.4
Cytosine; C6α
Uracil; C6α
Cytosine; C5α
Adenine; C8γ
Thymine; OCH
3
Cytosine; C6β Uracil; O
2β
Uracil; C6β
Experimental field / T
Theoretical field / T
ALC |∆M| = 0 resonance features
0.6 0.7 0.8 0.9 1.0 1.1 1.2 1.3 1.4 1.5
1.0
1.1
1.2
1.3
1.4
1.5
1.6
1.7
1.8
Uracil; O2
Thymine; O2
Uracil; O4
Experimental field / T
Theoretical field / T
ALC |∆M| = 1 O-Mu adduct resonance features
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1 2 3 4
-0.15
-0.10
-0.05
0.00
0.05
0.10
300K
Field / T
Derivative of polarisation
200K
20K
The ALC-µSR spectra ofdsDNA (Herring testes).
The resonance signals observed and assigned for the different bases are indicated as a stick diagram for comparison.
The predicted positions, using the DFT results and the linear correlations, of the other possible addition sites on the bases for which no experimental ALC signals were observed are indicated as dark squares.
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µµSRSR•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
Two main types of measurement:
(a) Active observer of a process
Radical formation modifies the process
(b) Passive observer of a process
Measured properties similar to close-shell compound
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µµSRSR•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
O
Diallylether
Mu
O
Mu•
O
Mu
•
Rates of Radical Cyclization
P. Burkhatd et. Al. J. Phys. Chem. 88 (1984) 773
k
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µµSRSR•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
TF-MuSR
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µµSRSR•• Molecules with Molecules with MuoniumMuonium [[µµ++ee--]]
k (338K) = 9.3 x 106 s-1
and compares well with the literature estimates of
k (338K) = 8.8 x 106 s-1
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µµSRSR
•• Muon Muon Spin RelaxationSpin Relaxation
sampleµ+
detectors
FB
Measure (F - B)/(F + B) vs Time
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Molecular Dynamics
Theory
( )222
22
ωτ1
τ.
x1
x.A2π2.λ
++= δ
( )ijij
2
ijij ω.φ.PMλ =
Coupling of perturbation
Change in muon polarisation
Spectral density of perturbation
S.F.J. Cox and D.S. Sivia, Hyperfine Interactions 87 (1994) 971
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H
MuFe
Mu
Fe
H
Mu
Fe
FERROCENE
Fe-Mu radical cp-Mu exo-radical
cp-Mu endo-radical
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1 10 100-0.5
0.0
0.5
1.0
1.5
2.0
2.5
3.0
3.5
4.0
4.5
Field / mT
Relaxation /
µs-1
Ferrocene 300K
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0 50 100 150 200 250 300 350 400 450
-0.5
0.0
0.5
1.0
1.5
2.0
2.5
3.0
3.5
Relaxation /
µs-1
Temperature / K
0 50 100 150 200 250 300 350 400-0.05
0.00
0.05
0.10
0.15
0.20
0.25
0.30
0.35
0.40
Relaxation /
µs-1
Temperature / K
ï
ï4 ï6 ï8
ï22
ï23
ï24
ï25
ï26
ï
ï
ïln(/
τ ï)ï(1000 / T) / K
ï-1
ï4 ï6 ï8 ï10 ï12 ï14ï22.0
ï22.5
ï23.0
ï23.5
ï24.0
ï24.5
ï25.0
ï25.5
ï26.0
ï
ï
ïln(1/τ ï)
ï(1000 / T) / Kï-1
∆E = 3.4(0.4) kJ mol-1
∆E = 5.8(0.4) kJ mol-1
Α = 6.3(1.7)x1011 s-1
Α = 1.1(0.4)x1012 s-1
Cp
-Mu
re
po
lari
ses
lik
e b
en
zen
eFe
-Mu
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e2u
e1g (xz,yz)
e2u
e1g
e1u
a1
a1 a1g
a1u
d(a1g,e1g,e2g)
e1g
e1u
e2g (x2-y2,xy)
a1g (z2)
e2u
e1g (xz,yz)
e2u
e1g
e1u
a1u
a1g a1g
a1u
d(a1g,e1g,e2g)
e1g
e1u
e2g (x2-y2,xy)
a1g (z2)
∆E = 5.8(0.4) kJ mol-1
Α = 1.1x1012(0.4) s-1
∆E = 3.4(0.4) kJ mol-1
Α = 6.3x1011(1.7) s-1
Agrees with NMR & QENS valuesfor cyclopentadienyl ring rotation
LUMO
LUMO
NON BONDING
ANTI BONDING
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I II IIIb IVb Vb VIb VIIb VIIIb Ib IIb III IV V VI VII 0
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 H He
Li Be B C N O F Ne Na Mg Al Si P S Cl Ar K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe Cs Ba La* Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn Fr Ra Ac** Rf Db Sg Bh Hs Mt Uun Uuu Uub Uuq Uuh Uuo
Lanthanides * Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Actinides ** Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr
Benzene chromium tricarbonyl
Cyclopentadienyl manganese tricarbonyl
Ferrocene
Ruthenocene
Osmocene
LUMO non-bonding
LUMO anti-bonding
Agree with NMR and QENS
Do not agree with NMR and QENS
Both types
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e2u
e1g (xz,yz)
e2u
e1g
e1u
a1
a1 a1g
a1u
d(a1g,e1g,e2g)
e1g
e1u
e2g (x2-y2,xy)
a1g (z2)
e2u
e1g (xz,yz)
e2u
e1g
e1u
a1u
a1g a1g
a1u
d(a1g,e1g,e2g)
e1g
e1u
e2g (x2-y2,xy)
a1g (z2)
∆E = 5.8(0.4) kJ mol-1
Α = 1.1(0.4) s-1
∆E = 3.4(0.4) kJ mol-1
Α = 6.3(1.7) s-1
Agrees with NMR & QENS values
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Photoelectron spectroscopic evidence to show the drop in energy of the d-orbitals across the Periodic Table.
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AcknowledgementsAcknowledgements
Julea Butt UEAVasily Oganesyan UEARoger Grinter UEA
Muon Group Members ISIS-RAL & PSI
John Stride UEAGina Aston UEAPenny Hubbard UEALaure Camus UEA
EPSRC for funding