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Definición y significado de bohrium

Definición

bohrium (n.)

1.a transuranic element

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definición de bohrium (Wikipedia)

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bohrium (n.)

transuranien (fr)[ClasseTaxo.]


Wikipedia

Bohrium

                   
seaborgiumbohriumhassium
Re

Bh

(Ups)
Appearance
unknown
General properties
Name, symbol, number bohrium, Bh, 107
Pronunciation Listeni/ˈbɔəriəm/
Element category transition metal
Group, period, block 77, d
Standard atomic weight [270]
Electron configuration [Rn] 5f14 6d5 7s2
(calculated)[1]
Electrons per shell 2, 8, 18, 32, 32, 13, 2
(predicted) (Image)
Physical properties
Atomic properties
Oxidation states 7
Ionization energies 1st: 740 (extrapolated)[1] kJ·mol−1
2nd: 1690 (extrapolated)[1] kJ·mol−1
3rd: 2570 (extrapolated)[1] kJ·mol−1
Covalent radius 141 (estimated)[2] pm
Miscellanea
CAS registry number 54037-14-8
Most stable isotopes
Main article: Isotopes of bohrium
iso NA half-life DM DE (MeV) DP
274Bh syn ~54 s[3] α 8.8 270Db
272Bh syn 9.8 s α 9.02 268Db
271Bh syn α 267Db
270Bh syn 61 s α 8.93 266Db
267Bh syn 17 s α 8.83 263Db
only half-times of over a second are included here
· r

Bohrium is a chemical element with the symbol Bh and atomic number 107 and is the heaviest member of group 7 (VIIB).

It is a synthetic element whose most stable known isotope, 270Bh, has a half-life of 61 seconds. Chemical experiments have confirmed bohrium's predicted position as a heavier homologue to rhenium with the formation of a stable +7 oxidation state.[4]

Contents

  History

  Official discovery

The first convincing synthesis was in 1981 by a German research team led by Peter Armbruster and Gottfried Münzenberg at the Gesellschaft für Schwerionenforschung (Institute for Heavy Ion Research, GSI) in Darmstadt using the Dubna reaction.

209
83
Bi
+ 54
24
Cr
262
107
Bh
+ n

In 1989, the GSI team successfully repeated the reaction during their efforts to measure an excitation function. During these experiments, 261Bh was also identified in the 2n evaporation channel and it was confirmed that 262Bh exists as two states - a ground state and an isomeric state.

The IUPAC/IUPAP Transfermium Working Group report in 1992 officially recognised the GSI team as discoverers of bohrium.

  Proposed names

Historically bohrium has been referred to as eka-rhenium.

The German group suggested the name nielsbohrium with symbol Ns to honor the Danish physicist Niels Bohr. The Soviet scientists had suggested this name be given to element 105 (which was finally called dubnium) and the German team wished to recognise both Bohr and the fact that the Dubna team had been the first to propose the cold fusion reaction.

There was an element naming controversy as to what the elements from 104 to 106 were to be called; the IUPAC adopted unnilseptium (symbol Uns) as a temporary, systematic element name for this element. In 1994 a committee of IUPAC recommended that element 107 be named bohrium, not nielsbohrium, since there was no precedence for using a scientist's complete name in the naming of an element.[5] This was opposed by the discoverers[citation needed] who were adamant that they had the right to name the element. The matter was handed to the Danish branch of IUPAC who voted in favour of the name bohrium. There was some concern however that the name might be confused with boron and in particular the distinguishing of the names of their respective oxo-ions bohrate and borate. Despite this, the name bohrium for element 107 was recognized internationally in 1997.[6] The IUPAC subsequently decided that bohrium salts should be called bohriates.

  Nucleosynthesis

  Cold fusion

This section deals with the synthesis of nuclei of bohrium by so-called "cold" fusion reactions. These are processes which create compound nuclei at low excitation energy (~10-20 MeV, hence "cold"), leading to a higher probability of survival from fission. The excited nucleus then decays to the ground state via the emission of one or two neutrons only.

209Bi(54Cr,xn)263-xBh (x=1,2)

The synthesis of bohrium was first attempted in 1976 by scientists at the Joint Institute for Nuclear Research at Dubna using this cold fusion reaction. Analysis was by detection of spontaneous fission (SF). They discovered two SF activities, one with a 1-2 ms half-life and one with a 5 s activity. Based on the results of other cold fusion reactions, they concluded that they were due to 261Bh and 257Db respectively. However, later evidence gave a much lower SF branching for 261Bh reducing confidence in this assignment. The assignment of the dubnium activity was later changed to 258Db, presuming that the decay of bohrium was missed. The 2 ms SF activity was assigned to 258Rf resulting from the 33% EC branch.[7] The GSI team studied the reaction in 1981 in their discovery experiments. Five atoms of 262Bh were detected using the method of correlation of genetic parent-daughter decays.[8] In 1987, an internal report from Dubna indicated that the team had been able to detect the spontaneous fission of 261Bh directly. The GSI team further studied the reaction in 1989 and discovered the new isotope 261Bh during the measurement of the 1n and 2n excitation functions but were unable to detect an SF branching for 261Bh.[9] They continued their study in 2003 using newly developed bismuth(III) fluoride (BiF3) targets, used to provide further data on the decay data for 262Bh and the daughter 258Db. The 1n excitation function was remeasured in 2005 by the team at LBNL after some doubt about the accuracy of previous data. They observed 18 atoms of 262Bh and 3 atoms of 261Bh and confirmed the two isomers of 262Bh. [10]

209Bi(53Cr,xn)262-xBh

The team at Dubna studied this reaction in 1976 in order to assist in their assignments of the SF activities from their experiments with a Cr-54 beam. They were unable to detect any such activity, indicating the formation of different isotopes decaying primarily by alpha decay.

209Bi(52Cr,xn)261-xBh (x=1)

This reaction was studied for the first time in 2007 by the team at LBNL to search for the lightest bohrium isotope 260Bh. The team successfully detected 8 atoms of 260Bh decaying by correlated 10.16 MeV alpha particle emission to 256Db. The alpha decay energy indicates the continued stabilising effect of the N=152 closed shell.[11]

208Pb(55Mn,xn)263-xBh (x=1)

The team at Dubna also studied this reaction in 1976 as part of their newly established cold fusion approach to new elements. As for the reaction using a Bi-209 target, they observed the same SF activities and assigned them to 261107 and 257105. Later evidence indicated that these should be reassigned to 258105 and 258104 (see above). In 1983, they repeated the experiment using a new technique: measurement of alpha decay from a descendant using chemical separation. The team were able to detect the alpha decay from a descendant of the 1n evaporation channel, providing some evidence for the formation of element 107 nuclei. This reaction was later studied in detail using modern techniques by the team at LBNL. In 2005 they measured 33 decays of 262Bh and 2 atoms of 261Bh, providing a 1n excitation function and some spectroscopic data of both 262Bh isomers. The 2n excitation function was further studied in a 2006 repeat of the reaction. [12] [13] The team found that this reaction had a higher 1n cross section than the corresponding reaction with a Bi-209 target, contrary to expectations. Further research is required to understand the reasons.

  Hot fusion

This section deals with the synthesis of nuclei of bohrium by so-called "hot" fusion reactions. These are processes which create compound nuclei at high excitation energy (~40-50 MeV, hence "hot"), leading to a reduced probability of survival from fission and quasi-fission. The excited nucleus then decays to the ground state via the emission of 3-5 neutrons.

238Am(31P,xn)269-xBh (x=5?)

This reaction was first studied in 2006 at the LBNL as part of their systematic study of fusion reactions using 238U targets. Results have not been published but preliminary results appear to indicate the observation of spontaneous fission, possibly from 264Bh.[14]

243Am(26Mg,xn)269-xBh (x=3,4,5)

Recently, the team at the Institute of Modern Physics (IMP), Lanzhou, have studied the nuclear reaction between americium-243 and magnesium-26 ions in order to synthesise the new isotope 265Bh [15] and gather more data on 266Bh. In two series of experiments, the team has measured partial excitation functions of the 3n,4n and 5n evaporation channels.

248Cm(23Na,xn)271-xBh (x=4,5)

This reaction was studied for the first time in 2008 by the team at RIKEN, Japan, in order to study the decay properties of 266Bh, which is a decay product in their claimed decay chains of ununtrium.[16] The decay of 266Bh by the emission of 9.05-9.23 MeV alpha particles was further confirmed in 2010.[17]

249Bk(22Ne,xn)271-xBh (x=4)

The first attempts to synthesize bohrium by hot fusion pathways were performed in 1979 by the team at Dubna. The reaction was repeated in 1983. In both cases, they were unable to detect any spontaneous fission from nuclei of bohrium. More recently, hot fusions pathways to bohrium have been re-investigated in order to allow for the synthesis of more long-lived, neutron rich isotopes to allow a first chemical study of bohrium. In 1999, the team at LBNL claimed the discovery of long-lived 267Bh (5 atoms) and 266Bh (1 atom).[18] Later, both of these were confirmed.[19] The team at the Paul Scherrer Institute (PSI) in Bern, Switzerland later synthesized 6 atoms of 267Bh in the first definitive study of the chemistry of bohrium (see below).

254Es(16O,xn)270-xBh

As an alternative means of producing long-lived bohrium isotopes suitable for a chemical study, the synthesis of 267Bh and 266Bh were attempted in 1995 by the team at GSI using the highly asymmetric reaction using an einsteinium-254 target. They were unable to detect any product atoms.

  As decay products

Isotopes of bohrium have also been detected in the decay of heavier elements. Observations to date are shown in the table below:

Evaporation Residue Observed Bh isotope
294Uus 274Bh
288Uup 272Bh
287Uup 271Bh
282Uut 270Bh
278Uut 266Bh
272Rg 264Bh
266Mt 262Bh

  Natural occurrence

The occurrence of bohrium in nature in such minerals as molybdenite is theoretically possible, though highly unlikely.[20]

  Isotopes

A total of eleven isotopes of bohrium have been characterized. The proton-rich isotopes with masses 260, 261, and 262 were directly produced by cold fusion, those with mass 262 and 264 were reported in the chains of the elements 109 and 111, while the neutron-rich isotopes with masses 266, 267 were created in irradiations of actinide targets. The four most neutron-rich ones with masses 270, 271, 272, and 274 appear in decay chains of 282113, 287115, 288115, and 294117 respectively. These ten isotopes have half-lives ranging from 8 miliseconds to 0.9 minute, and all undergo alpha-decay.[19]

Isotope Year discovered discovery reaction Half-times
260Bh 2007 209Bi(52Cr,n) [11]
261Bh 1989 209Bi(54Cr,2n)
262Bhg,m 1981 209Bi(54Cr,n)
263Bh unknown
264Bh 1994 209Bi(64Ni,n)
265Bh 2004[21] 243Am(26Mg,4n)
266Bh 2000[22] 209Bi(70Zn,n)
267Bh 2000[22] 249Bk(22Ne,4n)
268Bh unknown
269Bh unknown
270Bh 2006 237Np(48Ca,3n)
271Bh 2005? 243Am(48Ca,4n) (5 sec)[23]
272Bh 2005 243Am(48Ca,3n) 9.8 sec[23]
273Bh unknown
274Bh 2010 249Bk(48Ca,3n) ~54 sec[3]

  Nuclear isomerism

262Bh

The only confirmed example of isomerism in bohrium is for the isotope 262Bh. Direct production populates two states, a ground state and an isomeric state. The ground state is confirmed as decaying by alpha emission with alpha lines at 10.08,9.82 and 9.76 MeV with a revised half-life of 84 ms. The excited state decays by alpha emission with lines at 10.37 and 10.24 MeV with a revised half-life of 9.6 ms.

  Chemical properties

  Extrapolated

Bohrium is projected to be the fourth member of the 6d series of transition metals and the heaviest member of group VII in the Periodic Table, below manganese, technetium and rhenium. All the members of the group readily portray their group oxidation state of +7 and the state becomes more stable as the group is descended. Thus bohrium is expected to form a stable +7 state. Technetium also shows a stable +4 state whilst rhenium exhibits stable +4 and +3 states. Bohrium may therefore show these lower states as well.

The heavier members of the group are known to form volatile heptoxides M2O7, so bohrium should also form the volatile oxide Bh2O7. The oxide should dissolve in water to form perbohric acid, HBhO4. Rhenium and technetium form a range of oxyhalides from the halogenation of the oxide. The chlorination of the oxide forms the oxychlorides MO3Cl, so BhO3Cl should be formed in this reaction. Fluorination results in MO3F and MO2F3 for the heavier elements in addition to the rhenium compounds ReOF5 and ReF7. Therefore, oxyfluoride formation for bohrium may help to indicate eka-rhenium properties.

  Experimental

In 1995, the first report on attempted isolation of the element was unsuccessful.[24]

In 2000, it was confirmed that although relativistic effects are important, the 107th element does behave like a typical group 7 element.[25]

In 2000, a team at the PSI conducted a chemistry reaction using atoms of 267Bh produced in the reaction between Bk-249 and Ne-22 ions. The resulting atoms were thermalised and reacted with a HCl/O2 mixture to form a volatile oxychloride. The reaction also produced isotopes of its lighter homologues, technetium (as 108Tc) and rhenium (as 169Re). The isothermal adsorption curves were measured and gave strong evidence for the formation of a volatile oxychloride with properties similar to that of rhenium oxychloride. This placed bohrium as a typical member of group 7.[4]

2 Bh + 3 O2 + 2 HCl → 2 BhO3Cl + H2
Formula Name(s)
BhO3Cl bohrium oxychloride ; bohrium(VII) chloride trioxide

  See also


  References

  1. ^ a b c d Johnson, E.; Fricke, B.; Jacob, T.; Dong, C. Z.; Fritzsche, S.; Pershina, V. (2002). "Ionization potentials and radii of neutral and ionized species of elements 107 (bohrium) and 108 (hassium) from extended multiconfiguration Dirac–Fock calculations". The Journal of Chemical Physics 116: 1862. Bibcode 2002JChPh.116.1862J. DOI:10.1063/1.1430256. 
  2. ^ Chemical Data. Bohrium - Bh, Royal Chemical Society
  3. ^ a b 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. Bibcode 2010PhRvL.104n2502O. DOI:10.1103/PhysRevLett.104.142502. PMID 20481935.  (gives life-time of 1.3 min based on a single event; conversion to half-life is done by multiplying with ln(2).)
  4. ^ a b "Gas chemical investigation of bohrium (Bh, element 107)", Eichler et al., GSI Annual Report 2000. Retrieved on 2008-02-29
  5. ^ "Names and symbols of transfermium elements (IUPAC Recommendations 1994)". Pure and Applied Chemistry 66 (12): 2419. 1994. DOI:10.1351/pac199466122419. 
  6. ^ "Names and symbols of transfermium elements (IUPAC Recommendations 1997)". Pure and Applied Chemistry 69 (12): 2471. 1997. DOI:10.1351/pac199769122471. 
  7. ^ Barber, R. C.; Greenwood, N. N.; Hrynkiewicz, A. Z.; Jeannin, Y. P.; Lefort, M.; Sakai, M.; Ulehla, I.; Wapstra, A. P. et al. (1993). "Discovery of the transfermium elements. Part II: Introduction to discovery profiles. Part III: Discovery profiles of the transfermium elements (Note: for Part I see Pure Appl. Chem., Vol. 63, No. 6, pp. 879-886, 1991)". Pure and Applied Chemistry 65 (8): 1757. DOI:10.1351/pac199365081757. 
  8. ^ Münzenberg, G.; Hofmann, S.; He�berger, F. P.; Reisdorf, W.; Schmidt, K. H.; Schneider, J. H. R.; Armbruster, P.; Sahm, C. C. et al. (1981). "Identification of element 107 by α correlation chains". Zeitschrift für Physik A 300: 107. Bibcode 1981ZPhyA.300..107M. DOI:10.1007/BF01412623. 
  9. ^ Münzenberg, G.; Armbruster, P.; Hofmann, S.; Heßberger, F. P.; Folger, H.; Keller, J. G.; Ninov, V.; Poppensieker, K. et al. (1989). "Element 107". Zeitschrift für Physik A 333 (2): 163. Bibcode 1989ZPhyA.333..163M. DOI:10.1007/BF01565147. 
  10. ^ "Entrance Channel Effects in the Production of 262,261Bh", Nelson et al., LBNL repositories 2005. Retrieved on 2008-03-04
  11. ^ a b Nelson, S.; Gregorich, K.; Dragojević, I.; Garcia, M.; Gates, J.; Sudowe, R.; Nitsche, H. (2008). "Lightest Isotope of Bh Produced via the Bi209(Cr52,n)Bh260 Reaction". Physical Review Letters 100 (2). Bibcode 2008PhRvL.100b2501N. DOI:10.1103/PhysRevLett.100.022501. 
  12. ^ Folden Iii, C. M. (2006). "Excitation function for the production of 262Bh (Z=107) in the odd-Z-projectile reaction 208Pb(55Mn, n)". Physical Review C 73: 014611. Bibcode 2006PhRvC..73a4611F. DOI:10.1103/PhysRevC.73.014611. 
  13. ^ "Excitation function for the production of 262Bh (Z=107) in the odd-Z-projectile reaction 208Pb(55Mn, n)", Folden et al., LBNL repositories, May 19, 2005. Retrieved on 2008-02-29
  14. ^ Hot fusion studies at the BGS with light projectiles and 238U targets, J. M. Gates
  15. ^ Gan, Z.G.; Guo, J. S.; Wu, X. L.; Qin, Z.; Fan, H. M.; Lei, X. G.; Liu, H. Y.; Guo, B. et al. (2004). "New isotope 265Bh". The European Physical Journal A 20 (3): 385. Bibcode 2004EPJA...20..385G. DOI:10.1140/epja/i2004-10020-2. 
  16. ^ Morita, Kosuke; et al. (2009). "Decay Properties of 266Bh and 262Db Produced in the 248Cm + 23Na Reaction". Journal of the Physical Society of Japan 78 (6): 064201. arXiv:0904.1093. Bibcode 2009JPSJ...78f4201M. DOI:10.1143/JPSJ.78.064201. 
  17. ^ Morita, K.; Morimoto, K.; Kaji, D.; Haba, H.; Ozeki, K.; Kudou, Y.; Sato, N.; Sumita, T. et al. (2010). Decay Properties of [sup 266]Bh and [sup 262]Db Produced in the [sup 248]Cm+[sup 23]Na Reaction—Further Confirmation of the [sup 278]113 Decay Chain—. pp. 331. DOI:10.1063/1.3455961. 
  18. ^ Wilk, P. A.; Gregorich, KE; Turler, A; Laue, CA; Eichler, R; Ninov V, V; Adams, JL; Kirbach, UW et al. (2000). "Evidence for New Isotopes of Element 107: 266Bh and 267Bh". Physical Review Letters 85 (13): 2697–700. Bibcode 2000PhRvL..85.2697W. DOI:10.1103/PhysRevLett.85.2697. PMID 10991211. 
  19. ^ a b Münzenberg, G.; Gupta, M. (2011). Production and Identification of Transactinide Elements. pp. 877. DOI:10.1007/978-1-4419-0720-2_19. 
  20. ^ Ivanov, A. V. (2006). "The possible existence of Hs in nature from a geochemical point of view". Physics of Particles and Nuclei Letters 3 (3): 165. arXiv:nucl-th/0604052. Bibcode 2006PPNL....3..165I. DOI:10.1134/S1547477106030046. 
  21. ^ Gan, Z. G.; Guo, J. S.; Wu, X. L.; Qin, Z.; Fan, H. M.; Lei, X. G.; Liu, H. Y.; Guo, B. et al. (2004). "New isotope 265Bh". The European Physical Journal A 20 (3): 385. Bibcode 2004EPJA...20..385G. DOI:10.1140/epja/i2004-10020-2. 
  22. ^ a b Wilk, P.; Gregorich, K.; Türler, A.; Laue, C.; Eichler, R.; Ninov, V.; Adams, J.; Kirbach, U. et al. (2000). "Evidence for New Isotopes of Element 107: B266h and B267h". Physical Review Letters 85 (13): 2697–700. Bibcode 2000PhRvL..85.2697W. DOI:10.1103/PhysRevLett.85.2697. PMID 10991211. 
  23. ^ a b Oganessian, Yu.; Utyonkov, V.; Dmitriev, S.; Lobanov, Yu.; Itkis, M.; Polyakov, A.; Tsyganov, Yu.; Mezentsev, A. et al. (2005). "Synthesis of elements 115 and 113 in the reaction Am243+Ca48". Physical Review C 72 (3). Bibcode 2005PhRvC..72c4611O. DOI:10.1103/PhysRevC.72.034611. 
  24. ^ Malmbeck, R.; Skarnemark, G.; Alstad, J.; Fure, K.; Johansson, M.; Omtvedt, J. P. (2000). Journal of Radioanalytical and Nuclear Chemistry 246 (2): 349. DOI:10.1023/A:1006791027906. 
  25. ^ Gäggeler, H. W.; Eichler, R.; Brüchle, W.; Dressler, R.; Düllmann, Ch.E.; Eichler, B.; Gregorich, K. E.; Hoffman, D. C. et al. (2000). "Chemical characterization of bohrium (element 107)". Nature 407 (6800): 63–5. DOI:10.1038/35024044. PMID 10993071. 

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