/ Flashcards

1
Q

lewis acid

A

e- pair acceptor

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2
Q

lewis base

A

e- pair donor

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3
Q

enthalpic factors of the formation of metal-ion complexes

A

increased umber of ligands increases thermodynamic stability
increased bond strength increases thermodynamic stability
steric hinderance : number f ligands is limited by repulsion
increased charge reduces the stability of the complex

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4
Q

formation constant

A

Kf (M-1)

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5
Q

stability constant

A

B (beta)

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6
Q

hard acid/base

A

smaller and more difficult to polarize

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7
Q

polydentate

A

ligands with more than 1 donor atom which can bond to the metal ion

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8
Q

chelation

A

coordination of 2 or more donor atoms from a single ligand

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9
Q

chelate effect

A

reduced binding energy
increased binding affinity
increase in entropy compared to non-chelated ligands

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10
Q

n

A

hapticity = number of contiguous atoms of a ligand attachted to a metal

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11
Q

k

A

denticity = number of non-contiguous atoms coordinating from a ligand
often a chelating ligand

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12
Q

u

A

number of metal ions bridged by a ligand

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13
Q

normal geometry of a 2 coordinate complex

A

linear

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14
Q

normal geometry of a 3 coordinate complex

A

trigonal

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15
Q

normal geometry of a 4 coordinate complex

A

tetrahedral/square planar

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16
Q

normal geometry of a 5 coordinate complex

A

trigonal bipyramidal

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17
Q

normal geometry of a 6 coordinate complex

A

octahedral bipyramidal

18
Q

crystal field theory

A

assumes all metal ligand bonding is ionic

19
Q

crystal field theory

A

assumes all metal ligand bonding is ionic

20
Q

molecular orbital approach

A

assume all bonding is covalent between ligand and metal

21
Q

weak field ligands

A

pi bond donor ligands (lower splitting)

22
Q

strong field ligands

A

pi bond acceptor ligands (higher splitting)

23
Q

diamagnetic species

A

all e- are spin-paired
repelled by magnetic field
no overall magnetic moment

24
Q

paramagnetic species

A

1 or more unpaired e-
attracted by magnetic field (depends on no. of unpaired e-)
has magnetic moment

25
Q

ferromagnetic material

A

large domains of magnetic dipoles are aligned in the same direction
metal centre couple to increase para-magnetism

26
Q

antiferromagnetic material

A

neighboring magnetic dipoles are aligned in opposite directions
no overall magnetic field reduces para-magnetism

27
Q

eqn for effective magnetic moment

A

ueff = square root (n (n+2) )

28
Q

number of unpaired e- deduced from

A

increased weight of paramagnetic species

ueff when you have a change in weight and stoichiometry

29
Q

colour change of a complex caused by

A

change in oxidation state
change of ligand
change in coordination number or geometry

30
Q

where do the colours of transition metals arise from

A

absorption specific wavelengths of electromagnetic radiation in the visible region
absorptions arise from e- transitions between energy levels
between metal-centered orbitals or between metal+ligand centered molecular orbital

31
Q

lambda max

A

position and intensity of absorption peak

32
Q

effect of increased ionic radii on lambda max and energy required to promote an e-

A

lambda max decreases

E inreases

33
Q

effect of increased liagnd radii on lambda max and energy required to promote an e-

A
lambda max increases
E decreases (easier to oxidise)
34
Q

effect of increased oxidation state on lambda max and energy required to promote an e-

A
lambda max increases
E decreases (easier to reduce)
35
Q

electron paramagnetic resonance spectroscopy

A

micro electromagnetic radiation

detects spin state changes in substances with unpaired e- spins

36
Q

standard reduction potential

A

how easily an atom/ion can pick an e-
relative to standard H electrode
always in aqueous environment

37
Q

redox potential depends on

A

identity and oxidation state of metal ion

identity of ligand

38
Q

catalysis

A

redox between transition metal complex and small molecule oxidant/reductant

39
Q

e- transfer between complexes

A

redox
inner sphere - ligand shared and used as bridged intermediate
outer sphere - no bridging ligand

40
Q

ferromagnetism

A

permanently magnetized

41
Q

calculation of metal oxidation state

A

charge of complex - (no. ligands X ligand formal charge)