Zn, Cd and Hg Flashcards

1
Q

Why is it difficult to study the chemistry of Zinc complexes?

A
  • do not absorb in the visible region (unlike many transition metal complexes)
  • do not have isotopes that can be studied using NMR
  • diamagnetic - if you put a zinc complex in a magnetic field, they are weakly repelled
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2
Q

What are the characteristics of Zinc?

A
  • readily available in natural waters
  • exhibits no redox chemistry in nature
  • has a preference for o and N donors
  • catalyses acid-base reactions
  • Allows HO- to act as a base in biological systems
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3
Q

An example of a Zn enzyme

A
Carbonic anhydrase (CA)
• enhance transport if CO2
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4
Q

What is the main cause of symptoms in Alzheimer’s disease?

A

• alzheimer’s precursor protein - may be a copper protein which degrades into small pieces which ‘precipitate’ in the brian

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5
Q

How are chelating ligands different from their counterparts of lower denticity?

A
  • chelating ligands generally form more stable complexes
  • e.g. catecholate and enterobactin
  • also, Ni2+ complexes with NH3 and dien
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6
Q

Why may metal ions be toxic?

A
  1. involved in production of radicals
  2. cause precipitation of insoluble salts
  3. bind to proteins (enzymes) and disrupt their function
  4. displace essential metals from proteins - disruption of function
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7
Q

What is the criteria for an effective chelating agent?

A
  • must be soluble and non-toxic
  • should reach the tissue where metal toxicity is of concern
  • metal ligand complex formed should be stable and non-toxic
  • it should be selective for the metal of concern
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8
Q

How can metal ion toxicity effects be remediated?

A

the use of chelating agents

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9
Q

What is an example of a chelating agent?

A

H4EDTA - ethylenediamine tetraacetic acid

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10
Q

What is H4EDTA and describe its role

A

• hexadentate chelating agent - used to treat Pb poisoning

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11
Q

What is the problem with H4EDTA?

A
  • Binds to metals as the anion EDTA4-
  • bind to metals other than Pb such as Ca2+
  • hence, administered as the CaNa2EDTA to reduce calcium depletion
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12
Q

What is thalassemia?

A

A genetic disorder involving abnormal haemoglobin production

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13
Q

Treatment for thalassemia?

A
  • often requires blood transfusions leading to iron overload

* desferasirox in current clinical use to remove excess iron

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14
Q

How does desferasirox work?

A
  • it is a tridentate ligand - 2 ligands bound per iron atom
  • Fe3+ centre is octahedral
  • ONO chelating agent with both OH groups being deprotonated upon chelation
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15
Q

Denticity of desferasirox?

A

tridentate

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16
Q

What is the structure of the Fe3+ desferasirox complex?

A
  • Fe3+ centre - octahedral

* ONO donor atoms (O and N)

17
Q

Desferasirox function

A

Removes excess iron