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Bonds in Crystals
Bonds in Crystals
Results from the redistribution of e- that leads to a more
stable configuration between two or more atoms

The valence e- are those involved in bonding

When the e- have reorganized themselves, and if the
energy configuration is lower, then the atoms will stay
together

Electrical forces are chemical bonds, i.e., the attraction of
+ and - charges
Chemical bonds
Can belong to one of five principal bond types:
‣   ionic
‣   metallic
‣   covalent
‣   van der Waals
‣   hydrogen
Ionic, covalent, and metallic bonds involve valence e-,
while van der Waals and hydrogen bonds do not.
Ionic Bonds

 Ionic bond: forms when one or more e- in the
 valence shell of an atom are transferred to the
 valence shell of another, so that both
 elements achieve an noble gas configuration
Ionic Bonds
Na+         Cl-



      An idealized structure
      image with ionic
      bonding. The halite
      structure shown here
      represents bonding
      between Na and Cl.
Na+         Cl-



      An idealized structure
      image with ionic
      bonding. The halite
      structure shown here
      represents bonding
      between Na and Cl.
Ionic Bonds: Halite
Ionic Bond

The attraction between oppositely charged ions
constitutes the ionic (or electrostatic) bond

This bond forms as the result of the exchange of e-
(s) of the metal atom to the nonmetal atom
Ionic Bond
Ionic bonds commonly
form between atoms of
columns I and VII and
columns II and VI

As the distance (due to
the size of the anion)
increases, the bond
strength decreases, as a
function of increasing
inter-ionic distances
                           fig. 3.13
Ionic Bonds - Summary
  are generally of moderate hardness and have
  fairly high melting points
  are strong when forced together, but weak
  when cleaved or sheared
  are poor conductors of electricity and heat
  the symmetry of the resultant crystals is
  generally high
Metallic Bonds
  Metallic bond: the attractive force between
  positively charged nuclei with filled e- orbitals
  and the cloud of negative e- that holds such
  crystal structures together
Metallic Bonds
a) Schematic cross section
fig. 3.15
               through the structure of a
                metal. Each circle with a
             positive charge represents a
           nucleus with filled, nonvalence
            e- orbitals of the metal atoms.
           The mobile e- are represented
           by the cloud around the atoms
            (light gray). A possible e- path
           between the nuclei is shown by
           the line. b) An electron density
           map of copper atoms in copper
             metal showing the spherical
               nature and packing of the
           positively charged nuclei (white
             circles) surrounded by a less
               dense cloud of e- (contour
                          lines)
Covalent Bonds
 Covalent bond: when two (or more) atoms
 share their outer valence e-

 it is an intermediate bond type, between ionic
 and metallic
Covalent Bonds
The force of the bond is derived from the mutual
sharing of e-
Involves the merging and overlap of e- orbitals to
achieve an octet configuration



                               Cl-              Cl-
Covalent Bonds
The force of the bond is derived from the mutual
sharing of e-
Involves the merging and overlap of e- orbitals to
achieve an octet configuration



                               Cl-     Cl-
Covalent Bonds
Covalent Bonds
Covalent Bonds
Covalent Bonds
Elements near the middle of the periodic table, such
as C, Si, Al, and S, have 2, 3, and 4 vacancies in
their outer orbitals

# of covalent bonds = # of shared e-

The energy of the bonds produces a very rigid
structure - it is the strongest of all the chemical bonds
Covalent Bonds
 insoluble - generally slow reactivity
 chemical and mechanical stability
 very high melting points
 nonconductors of electricity
 the ions are no longer spherical, and the
 symmetry of the resulting crystals is likely
 to be lower
Electronegativity
 Ability of an atom in crystal structure or molecule to
 attract e- into its outer shell
 EN can be used as a basis for distinguishing
 elements:
 ‣   metals: < 1.9
 ‣   metalloid: 1.9 < X < 2.1
 ‣   non-metals: > 2.1
Electronegativity




            fig. 3.20
Electronegativity
An atom whose EN exceeds that of the other atom
by 2 or more, will generally be able to attract valence
e- from the other atom

If not a lot of contrast - nearly equal EN - neither
atom is able to capture an e- from the other; they
share
Bonds without Valence   e-



Van der Waals bond:
force of the bond is
derived from residual
surface charges on an
otherwise relatively
neutral structure
Van der Waals bonds
van der Waals Bond
Could be considered as a weak dipole effect

A small concentration of positive charge are one
end, leads to a small concentration of negative
charge at the other:
van der Waals Bond
 effective bonding over large distances in
 molecular structures

 generally defines a zone of cleavage and low
 hardness

 it is the weakest of the chemical bonds
Bonds without Valence                   e-


  Hydrogen bond: an electrostatic bond
  between a positively charged hydrogen ion
  and a negatively charged ion, such as O2- or
  N3-

  the hydrogen bond is considerably stronger
  than the van der Waals bond
Hydrogen bond
These bonds are weak, but there are many of them per
unit volume of structure, which results in an overall,
relatively strong material

Bonding is common in hydroxides (OH-)

Also present in many of the layer silicates, such as
micas and clay minerals
Bonds in Crystals
 In general, the stronger
 the average bond, the
 harder the crystal and the
 higher its melting point

 Hardness, cleavage,
 fusibility, electrical and
 thermal conductivity, and
 compressibility are all
 directly related to bond
 strength

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Lecture4 bonds

  • 2. Bonds in Crystals Results from the redistribution of e- that leads to a more stable configuration between two or more atoms The valence e- are those involved in bonding When the e- have reorganized themselves, and if the energy configuration is lower, then the atoms will stay together Electrical forces are chemical bonds, i.e., the attraction of + and - charges
  • 3. Chemical bonds Can belong to one of five principal bond types: ‣ ionic ‣ metallic ‣ covalent ‣ van der Waals ‣ hydrogen Ionic, covalent, and metallic bonds involve valence e-, while van der Waals and hydrogen bonds do not.
  • 4. Ionic Bonds Ionic bond: forms when one or more e- in the valence shell of an atom are transferred to the valence shell of another, so that both elements achieve an noble gas configuration
  • 6. Na+ Cl- An idealized structure image with ionic bonding. The halite structure shown here represents bonding between Na and Cl.
  • 7. Na+ Cl- An idealized structure image with ionic bonding. The halite structure shown here represents bonding between Na and Cl.
  • 9. Ionic Bond The attraction between oppositely charged ions constitutes the ionic (or electrostatic) bond This bond forms as the result of the exchange of e- (s) of the metal atom to the nonmetal atom
  • 10. Ionic Bond Ionic bonds commonly form between atoms of columns I and VII and columns II and VI As the distance (due to the size of the anion) increases, the bond strength decreases, as a function of increasing inter-ionic distances fig. 3.13
  • 11. Ionic Bonds - Summary are generally of moderate hardness and have fairly high melting points are strong when forced together, but weak when cleaved or sheared are poor conductors of electricity and heat the symmetry of the resultant crystals is generally high
  • 12. Metallic Bonds Metallic bond: the attractive force between positively charged nuclei with filled e- orbitals and the cloud of negative e- that holds such crystal structures together
  • 14. a) Schematic cross section fig. 3.15 through the structure of a metal. Each circle with a positive charge represents a nucleus with filled, nonvalence e- orbitals of the metal atoms. The mobile e- are represented by the cloud around the atoms (light gray). A possible e- path between the nuclei is shown by the line. b) An electron density map of copper atoms in copper metal showing the spherical nature and packing of the positively charged nuclei (white circles) surrounded by a less dense cloud of e- (contour lines)
  • 15. Covalent Bonds Covalent bond: when two (or more) atoms share their outer valence e- it is an intermediate bond type, between ionic and metallic
  • 16. Covalent Bonds The force of the bond is derived from the mutual sharing of e- Involves the merging and overlap of e- orbitals to achieve an octet configuration Cl- Cl-
  • 17. Covalent Bonds The force of the bond is derived from the mutual sharing of e- Involves the merging and overlap of e- orbitals to achieve an octet configuration Cl- Cl-
  • 21. Covalent Bonds Elements near the middle of the periodic table, such as C, Si, Al, and S, have 2, 3, and 4 vacancies in their outer orbitals # of covalent bonds = # of shared e- The energy of the bonds produces a very rigid structure - it is the strongest of all the chemical bonds
  • 22. Covalent Bonds insoluble - generally slow reactivity chemical and mechanical stability very high melting points nonconductors of electricity the ions are no longer spherical, and the symmetry of the resulting crystals is likely to be lower
  • 23. Electronegativity Ability of an atom in crystal structure or molecule to attract e- into its outer shell EN can be used as a basis for distinguishing elements: ‣ metals: < 1.9 ‣ metalloid: 1.9 < X < 2.1 ‣ non-metals: > 2.1
  • 24. Electronegativity fig. 3.20
  • 25. Electronegativity An atom whose EN exceeds that of the other atom by 2 or more, will generally be able to attract valence e- from the other atom If not a lot of contrast - nearly equal EN - neither atom is able to capture an e- from the other; they share
  • 26. Bonds without Valence e- Van der Waals bond: force of the bond is derived from residual surface charges on an otherwise relatively neutral structure
  • 27. Van der Waals bonds
  • 28. van der Waals Bond Could be considered as a weak dipole effect A small concentration of positive charge are one end, leads to a small concentration of negative charge at the other:
  • 29. van der Waals Bond effective bonding over large distances in molecular structures generally defines a zone of cleavage and low hardness it is the weakest of the chemical bonds
  • 30. Bonds without Valence e- Hydrogen bond: an electrostatic bond between a positively charged hydrogen ion and a negatively charged ion, such as O2- or N3- the hydrogen bond is considerably stronger than the van der Waals bond
  • 31. Hydrogen bond These bonds are weak, but there are many of them per unit volume of structure, which results in an overall, relatively strong material Bonding is common in hydroxides (OH-) Also present in many of the layer silicates, such as micas and clay minerals
  • 32.
  • 33. Bonds in Crystals In general, the stronger the average bond, the harder the crystal and the higher its melting point Hardness, cleavage, fusibility, electrical and thermal conductivity, and compressibility are all directly related to bond strength

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