inorganic chemistry

(Ben Green) #1

chemistry beyond the molecules, 48
double complex salts
3D crystalline supramolecular
network, 69
precipitation, 69
tectons, 67
toluene insertion, 69
X-ray crystal structure, 68f
micelles and vesicles
biexponential decays, 63– 64
luminescence quenching, 60
metallosupramolecular
amphiphilic block
copolymers, 61
metallosurfactants, 59
ring-opening metathesis
polymerization (ROMP), 61
Ruppz complex, 62
molecular systems
crystalline assemblies, 90– 91
1D arrays, 74– 77
2D arrays, 77– 81
3D networks, 81– 89
multivalency, 49
organometallic species, 49
photoactive arrays, 49– 50
photophysics
ground and excited-state
electronic wave, 50
Ir(III) complexes, 53
octahedral coordination
geometries, 52
Os(II) complexes, 53
Pd(II) complexes, 53– 54
properties, 51
Pt(II) complexes, 53– 54
Re(I) complexes, 53
spin–orbit coupling constant,
50 – 51
Stokes-shift, 52
zero-order electronic
configurations, 50– 51
photoresponsive assemblies,
noncovalent interactions
b-cyclodextrines, 56
host–guest assemblies, 55f
hydrogen bonds, 58f
interactions, 57– 58
organic chromophores, 54– 55


vectorial unidirectional
photoinduced energy transfer
process, 56
self-assembly, 48
Doping, 415– 416
XDouble complex salts
3D crystalline supramolecular
network, 69
precipitation, 69
tectons, 67
toluene insertion, 69
X-ray crystal structure, 68f

E
Electron–hole recombination,
410 – 411
Environmental
compartments–transition
metal transport
classification, photocatalysis,
295f
complexation effects
anthropogenic chelating
agents, 299
naturalchelating ligands,
296 – 299
sacrificial electron acceptor, 295
sunlight, 293– 296

F
Fenton reaction, 317– 318
Fermi level, 402– 403
First-order kinetics, 406– 407
Förster-cycle, acid–base equilibria,
254, 254f
Franck–Condon factor, 204– 205

G
Gibbs-energy change, 399–400, 399f

H
Hydride transfer shuttles, 263– 264

J
Jablonski diagram, 7f

L
Langmuir–Hinshelwood mechanism,
407 – 410, 409f

INDEX 433
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