
[After Lise MEITNER.]
The seventeenth of the synthetic transuranium elements. Element 109 falls in column 9 of the periodic table under the elements cobalt, rhodium, and iridium. It is expected to have chemical properties similar to those of iridium. See also Iridium; Periodic table; Transuranium elements.
Element 109 was discovered in 1982 by a team under P. Armbruster and G. Münzenberg at the Gesellschaft für Schwerionenforschung (GSI) at Darmstadt, Germany. In a sequence of bombardments of bismuth-209 targets with beams of ions of titanium-50, chromium-54, and iron-58, the compound systems 259105, 263107, and 267109 were produced. The decay analysis of the isotopes produced showed in the case of elements 105 and 107 the production of 258105 and 262107 by reaction channels in which one neutron is emitted. These isotopes have odd neutron and proton numbers and possess a special stability against spontaneous fission. It was shown that alpha-particle decay dominated the decay chains. Spontaneous fission occurs through a 30% electron capture branch of 256105 in 258104. Three decay chains were observed for the three reactions ending by fission of 258104, and the decay of the first atom of element 109 was observed. See also Dubnium; Nuclear reaction; Rutherfordium.
The single atom of element 109 was produced at a bombarding energy of 299 MeV in the reaction between iron-58 and bismuth-209. A total dose of 7 × 1017 ions was used to bombard thin layers of bismuth during a 250-h irradiation time.
In 1982 a German research team led by P. Armbruster and G. Münzenberg at the Institute for Heavy Ion Research at Darmstadt bombarded bismuth-209 atoms with iron-58 ions. On the tenth day of the experiment, one atom was unambiguously identified as an isotope of element 109 with mass number 266 and a half-life of 3.4 msec. The Germans suggested the name meitnerium to honor the Austrian-Swedish physicist and mathematician Lise Meitner. This name was recognized internationally in 1997.
See also synthetic elements; transuranium elements.
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| General properties | |||||||||||||||||||||||||||||||
| Name, symbol, number | meitnerium, Mt, 109 | ||||||||||||||||||||||||||||||
| Pronunciation | /maɪtˈnɪəriəm/ myet-NEER-ee-əm or /maɪtˈnɜriəm/ myet-NUR-ee-əm |
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| Element category | unknown | ||||||||||||||||||||||||||||||
| Group, period, block | 9, 7, d | ||||||||||||||||||||||||||||||
| Standard atomic weight | [278] | ||||||||||||||||||||||||||||||
| Electron configuration | [Rn] 7s2 5f14 6d7 (calculated)[2] |
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| Electrons per shell | 2, 8, 18, 32, 32, 15, 2 (predicted) (Image) |
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| Physical properties | |||||||||||||||||||||||||||||||
| Phase | solid (predicted[1]) | ||||||||||||||||||||||||||||||
| Atomic properties | |||||||||||||||||||||||||||||||
| Oxidation states | 3, 4, 6 (a guess based on that of iridium) |
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| Miscellanea | |||||||||||||||||||||||||||||||
| Crystal structure | face-centered cubic[1] | ||||||||||||||||||||||||||||||
| Magnetic ordering | paramagnetic[3] | ||||||||||||||||||||||||||||||
| CAS registry number | 54038-01-6 | ||||||||||||||||||||||||||||||
| Most stable isotopes | |||||||||||||||||||||||||||||||
| Main article: Isotopes of meitnerium | |||||||||||||||||||||||||||||||
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Meitnerium (
/maɪtˈnɪəriəm/ myt-NEER-ee-əm or /maɪtˈnɜriəm/ myt-NUR-ee-əm) is a chemical element with the symbol Mt and atomic number 109. It is placed as the heaviest member of group 9 (or VIII) in the periodic table but a sufficiently stable isotope is not known at this time which would allow chemical experiments to confirm its position as a heavier homologue to iridium, unlike its lighter neighbors. It was first synthesized in 1982 and several isotopes are currently known. The heaviest and the most stable isotope known is 278Mt, with a half-life of ~8 s.[4]
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Contents
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Meitnerium was first synthesized on August 29, 1982 by a German research team led by Peter Armbruster and Gottfried Münzenberg at the Institute for Heavy Ion Research (Gesellschaft für Schwerionenforschung) in Darmstadt.[5] The team bombarded a target of bismuth-209 with accelerated nuclei of iron-58 and detected a single atom of the isotope meitnerium-266:
Meitnerium was formerly known as unnilennium, bearing the symbol Une. Historically, meitnerium has been referred to as eka-iridium. The name meitnerium (Mt) was suggested in honor of the Austrian physicist Lise Meitner, a co-discoverer of protactinium (with Otto Hahn),[6][7][8][9][10] and one of the discoverers of nuclear fission.[11] In 1994 the name was recommended by IUPAC,[12] and was officially adopted in 1997.[13]
Super-heavy elements such as meitnerium are produced by bombarding lighter elements in particle accelerators that induces fusion reactions. Whereas most of the isotopes of meitnerium can be synthesized directly this way, some heavier ones have only been observed as decay products of elements with higher atomic numbers.[14]
After the first successful reaction of meitnerium in 1982 by the GSI team,[5] a team at FLNR, Dubna, also tried to observe the new element by bombarding bismuth-209 with iron-58. In 1985 they managed to identity alpha decays from the descendant isotope 246Cf indicating the formation of meitnerium. The observation of a further two atoms of 266Mt from the same reaction was reported in 1988 and of another 12 in 1997 by the German team at GSI.[15][16]
The same meitnerium isotope was also observed by the Russian team at Dubna in 1985 from the reaction:
by detecting the alpha decay of the descendant 246Cf nuclei. In 2007, an American team at LBNL confirmed the decay chain of 266Mt isotope from this reaction.[17]
A different reaction using tantalum-181 and krypton-86 was attempted in August 2001 at the GSI, but no evidence for formation of meitnerium via fusion could be observed.[citation needed] In 2002–2003, the team at LBNL attempted to generate the isotope 271Mt to study the chemical properties by bombarding uranium-238 with chlorine-37, but without success.[18] Other long-lived isotopes were unsuccessfully targeted by a team at Lawrence Livermore National Laboratory (LLNL) in 1988 by bombarding einsteinium-254 with neon-22.[18]
All the other isotopes of meitnerium have been detected only in the decay chains of the heavier elements. Since 1994, the following isotopes were observed:
| Isotope |
Half-life [22] |
Decay mode[22] |
Discovery year |
Reaction |
|---|---|---|---|---|
| 266Mt | 1.7 ms | α | 1982 | 209Bi(58Fe,n)[5] |
| 268Mt | 21 ms | α | 1994 | 272Rg(—,α)[21] |
| 270Mt | 5.0 ms | α | 2004 | 278Uut(—,2α)[23][19] |
| 274Mt | 0.44 s | α, SF | 2006 | 28tUup(—,2α)[19] |
| 275Mt | 9.7 ms | α | 2003 | 287Uup(—,3α)[19] |
| 276Mt | 0.72 s | α, SF | 2003 | 288Uup(—,3α)[19] |
| 278Mt | 8 s | α | 2009 | 294Uus(—,4α)[4] |
Only seven isotopes of meitnerium have been reported in the research literature. The longest lived one is 278Mt with a half-time of 8 seconds. A metastable nuclear isomer 270mMt has been reported to also have a half-life of over a second. Isotopes 276Mt and 274Mt have a half-life of 0.72 and 0.44 seconds respectively. The remaining four isotopes have a half life between 1 and 20 milliseconds.[22] The isotope 281Mt has been predicted to be the most likely stable one towards β-decay.[24]
Two atoms of 270Mt have been identified in the decay chains of 278Uut. The two decays have very different lifetimes and decay energies and are also produced from two apparently different isomers in 274Rg. The first isomer decays by emission of an 10.03 MeV alpha particle with a lifetime 7.2 ms. The other decays by emitting an alpha particle with a lifetime of 1.63 s. An assignment to specific levels is not possible with the limited data available. Further research is required.
The alpha decay spectrum for 268Mt appears to be complicated from the results of several experiments. Alpha lines of 10.28,10.22 and 10.10 MeV have been observed. Half-lives of 42 ms, 21 ms and 102 ms have been determined. The long-lived decay is associated with alpha particles of energy 10.10 MeV and must be assigned to an isomeric level. The discrepancy between the other two half-lives has yet to be resolved. An assignment to specific levels is not possible with the data available and further research is required.
Unambiguous determination of chemical character of meitnerium has yet to have been established due to two reasons: lack of sufficiently long-lived isotope, and a limited amount of likely volatile compounds that could be studies on a very small scale. However, the IrF6 fluoride is volatile above 60 ºC and therefore the identical compound of meitnerium might also be sufficiently volatile. However, since element 112 has been shown to be a transition metal, it is expected that all the elements in the 104–111 range would form a fourth transition metal series, with meitnerium as part of the platinum group metals.[9] Only extrapolated chemical properties are available for meitnerium.
Meitnerium is projected to be the sixth member of the 6d series of transition metals and the heaviest member of group 9 in the Periodic Table, below cobalt, rhodium and iridium. This group of transition metals is the first to show lower oxidation states and the +9 state is not known. The latter two members of the group show a maximum oxidation state of +6, whilst the most stable states are +4 and +3 for iridium and +3 for rhodium. Meitnerium is therefore expected to form a stable +3 state but may also portray stable +4 and +6 states.[citation needed] The oxidation state +9 might also be possible for meitnerium.[25]
The +VI state in group 9 is known only for the fluorides which are formed by direct reaction. Therefore, meitnerium should form a hexafluoride, MtF6. This fluoride is expected to be more stable than iridium(VI) fluoride, as the +6 state becomes more stable as the group is descended.[citation needed]
In combination with oxygen, rhodium forms Rh2O3 whereas iridium is oxidised to the +4 state in IrO2. Meitnerium may therefore show a dioxide, MtO2, if eka-iridium reactivity is shown.[citation needed]
The +3 state in group 9 is common in the trihalides (except fluorides) formed by direct reaction with halogens. Meitnerium should therefore form MtCl3, MtBr3 and MtI3 in an analogous manner to iridium.[citation needed] The tetrahalides have been predicted to have similar stabilities as those of iridium.[26]
Theoreticians have predicted the covalent radius of meitnerium to be 6 to 10 pm larger than that of iridium.[27] For example, the Mt–O bond distance is expected to be around 1.9 Å.[28]
Meitnerium is expected to be a solid under normal conditions and assume a face-centered-cubic crystal structure.[1]
Mt should be a very heavy metal with a density around 30 g/cm3 (Co: 8.9, Rh: 12.5, Ir: 22.5) and a high melting point around 2600–2900°C (Co: 1480, Rh: 1966, Ir: 2454). It should be very corrosion-resistant; even more so than Ir which is currently the most corrosion-resistant metal known.[citation needed]
The atomic electronic configuration is predicted to be [Rn] 5f14 6d7 7s2.[28]
| Periodic table | ||||||||||||||||||||||||||||||||||||||||||
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| H | He | |||||||||||||||||||||||||||||||||||||||||
| Li | Be | B | C | N | O | F | Ne | |||||||||||||||||||||||||||||||||||
| Na | Mg | Al | Si | P | S | Cl | Ar | |||||||||||||||||||||||||||||||||||
| K | Ca | Sc | Ti | V | Cr | Mn | Fe | Co | Ni | Cu | Zn | Ga | Ge | As | Se | Br | Kr | |||||||||||||||||||||||||
| Rb | Sr | Y | Zr | Nb | Mo | Tc | Ru | Rh | Pd | Ag | Cd | In | Sn | Sb | Te | I | Xe | |||||||||||||||||||||||||
| Cs | Ba | La | Ce | Pr | Nd | Pm | Sm | Eu | Gd | Tb | Dy | Ho | Er | Tm | Yb | Lu | Hf | Ta | W | Re | Os | Ir | Pt | Au | Hg | Tl | Pb | Bi | Po | At | Rn | |||||||||||
| Fr | Ra | Ac | Th | Pa | U | Np | Pu | Am | Cm | Bk | Cf | Es | Fm | Md | No | Lr | Rf | Db | Sg | Bh | Hs | Mt | Ds | Rg | Cn | Uut | Uuq | Uup | Uuh | Uus | Uuo | |||||||||||
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