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    Báo tài liệu có sai sót
    Nhắn tin cho tác giả
    (Tài liệu chưa được thẩm định)
    Nguồn:
    Người gửi: Đặng Công Anh Tuấn (trang riêng)
    Ngày gửi: 07h:49' 17-12-2008
    Dung lượng: 282.0 KB
    Số lượt tải: 14
    Số lượt thích: 0 người
    The d block:
    The d block consists of three horizontal series in periods 4, 5 & 6
    10 elements in each series
    Chemistry is “different” from other elements
    Special electronic configurations important
    Differences within a group in the d block are less sharp than in s & p block
    Similarities across a period are greater
    Visit www.worldofteaching.com
    For 100’s of free powerpoints
    Electronic Configuration
    Across the 1st row of the d block (Sc to Zn) each element
    has 1 more electron and 1 more proton
    Each “additional” electron enters the 3d sub-shell
    The core configuration for all the period 4 transition elements is that of Ar
    1s22s22p63s23p6
    1s
    2s
    3s
    4s
    2p
    3p
    3d
    Energy
    Ar
    1s2 2s2 2p6 3s2 3p6
    4p
    1s
    2s
    3s
    4s
    2p
    3p
    3d
    Energy
    Sc
    1s2 2s2 2p6 3s2 3p6 3d1 4s2
    4p
    Chromium and Copper
    Cr and Cu don’t fit the pattern of building up the 3d sub-shell, why?
    In the ground state electrons are always arranged to give lowest total energy
    Electrons are negatively charged and repel each other
    Lower total energy is obtained with e- singly in orbitals rather than if they are paired in an orbital
    Energies of 3d and 4s orbitals very close together in Period 4
    Chromium and Copper
    At Cr
    Orbital energies such that putting one e- into each 3d and 4s orbital gives lower energy than having 2 e- in the 4s orbital
    At Cu
    Putting 2 e- into the 4s orbital would give a higher energy than filling the 3d orbitals
    1s
    2s
    3s
    4s
    2p
    3p
    3d
    Energy
    Cr
    1s2 2s2 2p6 3s2 3p6 3d5 4s1
    4p
    1s
    2s
    3s
    4s
    2p
    3p
    3d
    Energy
    Cu
    1s2 2s2 2p6 3s2 3p6 3d10 4s1
    4p
    What is a transition metal?
    Transition metals [TM’s] have characteristic properties
    e.g. coloured compounds, variable oxidation states
    These are due to presence of an inner incomplete d sub-shell
    Electrons from both inner d sub-shell and outer s sub-shell can be involved in compound formation
    What is a transition metal?
    Not all d block elements have incomplete d sub-shells
    e.g. Zn has e.c. of [Ar]3d104s2, the Zn2+ ion ([Ar] 3d10) is not a typical TM ion
    Similarly Sc forms Sc3+ which has the stable e.c of Ar. Sc3+ has no 3d electrons
    What is a transition metal?
    For this reason, a transition metal is defined as being an element which forms at least one ion with a partially filled sub-shell of d electrons.
    In period 4 only Ti-Cu are TM’s!
    Note that when d block elements form ions the s electrons are lost first
    What are TM’s like?
    TM’s are metals
    They are similar to each other but different from s block metals eg Na and Mg
    Properties of TM’s
    Dense metals
    Have high Tm and Tb
    Tend to be hard and durable
    Have high tensile strength
    Have good mechanical properties
    What are TM’s like?
    Properties derive from strong metallic bonding
    TM’s can release e- into the pool of mobile electrons from both outer and inner shells
    Strong metallic bonds formed between the mobile pool and the +ve metal ions
    Enables widespread use of TMs!
    Alloys very important: inhibits slip in crystal lattice usually results in increased hardness and reduced malleability

    Effect of Alloying on TM’s
    TM Chemical Properties
    Typical chemical properties of the TM’s are
    Formation of compounds in a variety of oxidation states
    Catalytic activity of the elements and their compounds
    Strong tendency to form complexes
    See CI 11.6
    Formation of coloured compounds
    See CI 11.6

    Variable Oxidation States
    TM’s show a great variety of oxidation states cf s block metals
    If compare successive ionisation enthalpies (Hi) for Ca and V as follows
    M(g)  M+(g) + e- Hi(1)
    M+(g)  M2+(g) + e- Hi(2)
    M2+(g)  M3+(g) + e- Hi(3)
    M3+(g)  M4+(g) + e- Hi(4)
    Hi for Ca and V
    Hi for Ca and V
    Both Ca & V always lose the 4s electrons
    For Ca
    Hi(1) & Hi(2) relatively low as corresponds to removing outer 4s e-
    Sharp increase in Hi(3) & Hi(4) cf Hi(2) due to difficulty in removing 3p e-
    For Sc
    Gradual increase from Hi(1) to Hi(4) as removing 4s then 3d e-
    Oxidation States of TM’s
    In the following table
    Most important OS’s in boxes
    OS = +1 only important for Cu
    In all others sum of Hi(1) + Hi(2) low enough for 2e- to be removed
    OS = +2, where 4s e- lost shown by all except for Sc and Ti
    OS = +3, shown by all except Zn
    Oxidation States of TM’s
    Oxidation States of TM’s
    No of OS’s shown by an element increases from Sc to Mn
    In each of these elements highest OS is equal to no. of 3d and 4s e-
    After Mn decrease in no. of OS’s shown by an element
    Highest OS shown becomes lower and less stable
    Seems increasing nuclear charge binds 3d e- more strongly, hence harder to remove
    Oxidation States of TM’s
    In general
    Lower OS’s found in simple ionic compounds
    E.g. compounds containing Cr3+, Mn2+, Fe3+, Cu2+ ions
    TM’s in higher OS’s usually covalently bound to electronegative element such as O or F
    E.g VO3-, vanadate(V) ion; MnO4-, manganate(VII) ion
    Simple ions with high OS’s such as V5+ & Mn7+ are not formed
    Stability of OS’s
    Change from one OS to another is a redox reaction
    Relative stability of different OS’s can be predicted by looking at Standard Electrode Potentials
    E values

    Stability of OS’s
    General trends
    Higher OS’s become less stable relative to lower ones on moving from left to right across the series
    Compounds containing TM’s in high OS’s tend to be oxidising agents e.g MnO4-
    Compounds with TM’s in low OS’s are often reducing agents e.g V2+ & Fe2+
    Stability of OS’s
    General trends (continued)
    Relative stability of +2 state with respect to +3 state increases across the series
    For compounds early in the series, +2 state highly reducing
    E.g. V2+(aq) & Cr2+(aq) strong reducing agents
    Later in series +2 stable, +3 state highly oxidising
    E.g. Co3+ is a strong oxidising agent, Ni3+ & Cu3+ do not exist in aqueous solution.
    Catalytic Activity
    TM’s and their compounds effective and important catalysts
    Industrially and biologically!!
    The “people in the know” believe
    catalysts provide reaction pathway with lower EA than uncatalysed reaction (see CI 10.5)
    Once again,
    availability of 3d and 4s e-
    ability to change OS
    among factors which make TM’s such good catalysts
    Heterogeneous Catalysis
    Catalyst in different phase from reactants
    Usually means solid TM catalyst with reactants in liquid or gas phases
    TM’s can
    use the 3d and 4s e- of atoms on metal surface to from weak bonds to the reactants.
    Once reaction has occurred on TM surface, these bonds can break to release products
    Important example is hydrogenation of alkenes using Ni or Pt catalyst
    Heterogeneous Catalysis
    Homogeneous Catalysis
    Catalyst in same phase as reactants
    Usually means reaction takes place in aqueous phase
    Catalyst aqueous TM ion
    Usually involves
    TM ion forming intermediate compound with ome or more of the reactants
    Intermediate then breaks down to form products
    Homogeneous Catalysis
    Above reaction is that used in Activity SS5.2
    2,3-dihydroxybutanoate ion with hydrogen peroxide
    Reaction catalysed by Co2+

    Suggested Mechanism
    REACTANTS
    H2O2 +
    -O2CCH(OH)CH(OH)C02-
    Co2+ (pink)
    INTERMEDIATE
    containing
    Co3+ (green)
    PRODUCTS
    CO2, methanoate, H2O
    Co2+ (pink)
     
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