meitnerium

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(mīt-nûr'ē-əm) pronunciation
n. (Symbol Mt)
An artificially produced radioactive element with atomic number 109 that has known isotopes with mass numbers ranging from 265 to 279. The isotope with the longest confirmed half-life (0.7 seconds) is Mt 268. Also called unnilennium.

[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.


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meitnerium (mītnĭr'ēəm), artificially produced radioactive chemical element; symbol Mt; at. no. 109; mass number of most stable isotope 266; m.p., b.p., sp. gr., and valence unknown. Situated in Group 9 of the periodic table it is expected to have properties similar to those of iridium.

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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hassiummeitneriumdarmstadtium
Ir

Mt

(Upe)
Appearance
unknown
General properties
Name, symbol, number meitnerium, Mt, 109
Pronunciation /mtˈnɪəriəm/
myet-NEER-ee-əm
or /mtˈnɜriəm/
myet-NUR-ee-əm
Element category unknown
Group, period, block 97, d
Standard atomic weight [278]
Electron configuration [Rn] 7s2 5f14 6d7
(calculated)[2]
Electrons per shell 2, 8, 18, 32, 32, 15, 2
(predicted) (Image)
Physical properties
Phase solid (predicted[1])
Atomic properties
Oxidation states 3, 4, 6
(a guess based on that of iridium)
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
iso NA half-life DM DE (MeV) DP
278Mt syn 7.6 s α 9.6 274Bh
276Mt syn 0.72 s α 9.71 272Bh
274Mt syn 0.44 s α 9.76 270Bh
270mMt ? syn 1.1 s α 266Bh
· r

Meitnerium (play /mtˈnɪəriəm/ myt-NEER-ee-əm or /mtˈnɜriəm/ 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]

Contents

History

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:

209
83
Bi
+ 58
26
Fe
266
109
Mt
+ n

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]

Nucleosynthesis

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:

208
82
Pb
+ 59
27
Co
266
109
Mt
+ n

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:

  • 278Mt in the decay chain of 294Uus;[4]
  • 276Mt in the decay chain of 288Uup;[19]
  • 275Mt in the decay chain of 287Uup;[19]
  • 274Mt in the decay chain of 282Uut;[19]
  • 270Mt in the decay chain of 278Uut;[20]
  • 268Mt in the decay chain of 272Rg.[21]

Isotopes

List of meitnerium isotopes
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]

Nuclear isomerism

270Mt

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.

268Mt

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.

Properties

Chemical

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.

Oxidation states

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]

Chemistry

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]

Physical and atomic

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]

References

  1. ^ a b c Östlin, A.; Vitos, L. (2011). "First-principles calculation of the structural stability of 6d transition metals". Physical Review B 84 (11). Bibcode 2011PhRvB..84k3104O. doi:10.1103/PhysRevB.84.113104. 
  2. ^ Thierfelder, C.; Schwerdtfeger, P.; Heßberger, F. P.; Hofmann, S. (2008). "Dirac-Hartree-Fock studies of X-ray transitions in meitnerium". The European Physical Journal A 36 (2): 227. Bibcode 2008EPJA...36..227T. doi:10.1140/epja/i2008-10584-7. 
  3. ^ Saito, Shiro L. (2009). "Hartree–Fock–Roothaan energies and expectation values for the neutral atoms He to Uuo: The B-spline expansion method". Atomic Data and Nuclear Data Tables 95 (6): 836. Bibcode 2009ADNDT..95..836S. doi:10.1016/j.adt.2009.06.001. 
  4. ^ a b c Oganessian, Yu. Ts.; Abdullin, F. Sh.; Bailey, P. D.; Benker, D. E.; Bennett, M. E.; Dmitriev, S. N.; Ezold, J. G.; Hamilton, J. H. et al (2010). "Synthesis of a New Element with Atomic Number Z=117". Physical Review Letters 104 (14): 142502. Bibcode 2010PhRvL.104n2502O. doi:10.1103/PhysRevLett.104.142502. PMID 20481935. 
  5. ^ a b c Münzenberg, G.; Armbruster, P.; Heßberger, F. P.; Hofmann, S.; Poppensieker, K.; Reisdorf, W.; Schneider, J. H. R.; Schneider, W. F. W. et al (1982). "Observation of one correlated α-decay in the reaction 58Fe on 209Bi→267109". Zeitschrift für Physik A 309 (1): 89. Bibcode 1982ZPhyA.309...89M. doi:10.1007/BF01420157. 
  6. ^ Bentzen, S. M. (2000). "Lise Meitner and Niels Bohr--a historical note". Acta oncologica (Stockholm, Sweden) 39 (8): 1002–1003. PMID 11206992.  edit
  7. ^ Kyle, R. A.; Shampo, M. A. (1981). "Lise Meitner". JAMA: the Journal of the American Medical Association 245 (20): 2021. PMID 7014939.  edit
  8. ^ Frisch, O. R. (1973). "Distinguished Nuclear Pioneer--1973. Lise Meitner". Journal of nuclear medicine : official publication, Society of Nuclear Medicine 14 (6): 365–371. PMID 4573793.  edit
  9. ^ a b Griffith, W. P. (2008). "The Periodic Table and the Platinum Group Metals". Platinum Metals Review 52 (2): 114. doi:10.1595/147106708X297486. 
  10. ^ Rife, Patricia (2003). "Meitnerium". Chemical & Engineering News 81 (36): 186. doi:10.1021/cen-v081n036.p186. 
  11. ^ Wiesner, Emilie; Settle, Frank A. (2001). "Politics, Chemistry, and the Discovery of Nuclear Fission". Journal of Chemical Education 78 (7): 889. Bibcode 2001JChEd..78..889W. doi:10.1021/ed078p889. 
  12. ^ "Names and symbols of transfermium elements (IUPAC Recommendations 1994)". Pure and Applied Chemistry 66 (12): 2419. 1994. doi:10.1351/pac199466122419. 
  13. ^ Rayner-Canham, Geoff; Zheng, Zheng (2007). "Naming elements after scientists: An account of a controversy". Foundations of Chemistry 10: 13. doi:10.1007/s10698-007-9042-1. 
  14. ^ Armbruster, Peter & Munzenberg, Gottfried (1989). "Creating superheavy elements". Scientific American 34: 36–42. 
  15. ^ Münzenberg, G.; Hofmann, S.; Heßberger, F. P.; Folger, H.; Ninov, V.; Poppensieker, K.; Quint, A. B.; Reisdorf, W. et al (1988). "New results on element 109". Zeitschrift für Physik A 330 (4): 435. Bibcode 1988ZPhyA.330..435M. doi:10.1007/BF01290131. 
  16. ^ Hofmann, S.; Heßberger, F.P.; Ninov, V.; Armbruster, P.; Münzenberg, G.; Stodel, C.; Popeko, A.G.; Yeremin, A.V. et al (1997). "Excitation function for the production of 265 108 and 266 109". Zeitschrift für Physik A 358 (4): 377. Bibcode 1997ZPhyA.358..377H. doi:10.1007/s002180050343. 
  17. ^ Nelson et al (2009). "Comparison of complementary reactions in the production of Mt". Physical Rev. C 79 (2): 027605. Bibcode 2009PhRvC..79b7605N. doi:10.1103/PhysRevC.79.027605. 
  18. ^ a b "The search for 271Mt via the reaction 238U + 37Cl", Zielinski et al.., GSI Annual report, 2003. Retrieved on 2008-03-01
  19. ^ a b c d e f g Oganessian, Yu. Ts.; Penionzhkevich, Yu. E.; Cherepanov, E. A. (2007). "Heaviest Nuclei Produced in 48Ca-induced Reactions (Synthesis and Decay Properties)". AIP Conference Proceedings. 912. pp. 235. doi:10.1063/1.2746600. 
  20. ^ Morita, Kosuke; Morimoto, Kouji; Kaji, Daiya; Akiyama, Takahiro; Goto, Sin-Ichi; Haba, Hiromitsu; Ideguchi, Eiji; Kanungo, Rituparna et al (2004). "Experiment on the Synthesis of Element 113 in the Reaction 209Bi(70Zn,n)278113". Journal of the Physics Society Japan 73 (10): 2593. Bibcode 2004JPSJ...73.2593M. doi:10.1143/JPSJ.73.2593. 
  21. ^ a b Hofmann, S.; Ninov, V.; Heßberger, F. P.; Armbruster, P.; Folger, H.; Münzenberg, G.; Schött, H. J.; Popeko, A. G. et al (1995). "The new element 111". Zeitschrift für Physik A 350 (4): 281. Bibcode 1995ZPhyA.350..281H. doi:10.1007/BF01291182. 
  22. ^ a b c Sonzogni, Alejandro. "Interactive Chart of Nuclides". National Nuclear Data Center: Brookhaven National Laboratory. http://www.nndc.bnl.gov/chart/reCenter.jsp?z=104&n=158. Retrieved 2008-06-06. 
  23. ^ Morita, Kosuke; Morimoto, Kouji; Kaji, Daiya; Akiyama, Takahiro; Goto, Sin-Ichi; Haba, Hiromitsu; Ideguchi, Eiji; Kanungo, Rituparna et al (2004). "Experiment on the Synthesis of Element 113 in the Reaction209Bi(70Zn, n)278113". Journal of the Physical Society of Japan 73 (10): 2593. Bibcode 2004JPSJ...73.2593M. doi:10.1143/JPSJ.73.2593. 
  24. ^ http://xxx.lanl.gov/pdf/nucl-th/0512023.pdf
  25. ^ Himmel, Daniel; Knapp, Carsten; Patzschke, Michael; Riedel, Sebastian (2010). "How Far Can We Go? Quantum-Chemical Investigations of Oxidation State +IX". ChemPhysChem 11 (4): 865–9. doi:10.1002/cphc.200900910. PMID 20127784. 
  26. ^ Ionova, G. V.; Ionova, I. S.; Mikhalko, V. K.; Gerasimova, G. A.; Kostrubov, Yu. N.; Suraeva, N. I. (2004). "Halides of Tetravalent Transactinides (Rf, Db, Sg, Bh, Hs, Mt, 110th Element): Physicochemical Properties". Russian Journal of Coordination Chemistry 30 (5): 352. doi:10.1023/B:RUCO.0000026006.39497.82. 
  27. ^ Pyykkã, Pekka; Atsumi, Michiko (2009). "Molecular Double-Bond Covalent Radii for Elements Li—E112". Chemistry - A European Journal 15 (46): 12770. doi:10.1002/chem.200901472. 
  28. ^ a b Van Lenthe, E.; Baerends, E. J. (2003). "Optimized Slater-type basis sets for the elements 1-118". Journal of Computational Chemistry 24 (9): 1142–56. doi:10.1002/jcc.10255. PMID 12759913. 

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Mt (element)
Hassium (inorganic chemistry)
Lise Meitner (Austrian-Swedish physicist & mathematician)