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Nobelium, 102No
Mass number[259]
Nobelium in the periodic table
Periodperiod 7
Element category  Actinide
Electron configuration[Rn] 5f14 7s2
Electrons per shell2, 8, 18, 32, 32, 8, 2
Physical properties
Phase at STPsolid (predicted)[1]
Melting point1100 K ​(827 °C, ​1521 °F) (predicted)[1]
Density (near r.t.)9.9(4) g/cm3(predicted)[2]
Atomic properties
Oxidation states+2, +3
ElectronegativityPauling scale: 1.3 (predicted)[3]
Ionization energies
  • 1st: 639[4] kJ/mol
  • 2nd: 1254.3 kJ/mol
  • 3rd: 2605.1 kJ/mol
  • (all but first estimated)
Other properties
Natural occurrencesynthetic
Crystal structureface-centered cubic (fcc)
Face-centered cubic crystal structure for nobelium

CAS Number10028-14-5
Namingafter Alfred Nobel
DiscoveryJoint Institute for Nuclear Research
Main isotopes of nobelium
Iso­tope Abun­dance Half-life (t1/2) Decay mode Pro­duct
253No syn 1.6 min 80% ? 249Fm
20% ?+ 253Md
254No syn 51 s 90% ? 250Fm
10% ?+ 254Md
255No syn 3.1 min 61% ? 251Fm
39% ?+ 255Md
257No syn 25 s 99% ? 253Fm
1% ?+ 257Md
259No syn 58 min 75% ? 255Fm
25% ? 259Md
<10% SF
Category Category: Nobelium
| references

Nobelium is a synthetic chemical element with the symbol No and atomic number 102. It is named in honor of Alfred Nobel, the inventor of dynamite and benefactor of science. A radioactive metal, it is the tenth transuranic element and is the penultimate member of the actinide series. Like all elements with atomic number over 100, nobelium can only be produced in particle accelerators by bombarding lighter elements with charged particles. A total of twelve nobelium isotopes are known to exist; the most stable is 259No with a half-life of 58 minutes, but the shorter-lived 255No (half-life 3.1 minutes) is most commonly used in chemistry because it can be produced on a larger scale.

Chemistry experiments have confirmed that nobelium behaves as a heavier homolog to ytterbium in the periodic table. The chemical properties of nobelium are not completely known: they are mostly only known in aqueous solution. Before nobelium's discovery, it was predicted that it would show a stable +2 oxidation state as well as the +3 state characteristic of the other actinides: these predictions were later confirmed, as the +2 state is much more stable than the +3 state in aqueous solution and it is difficult to keep nobelium in the +3 state.

In the 1950s and 1960s, many claims of the discovery of nobelium were made from laboratories in Sweden, the Soviet Union, and the United States. Although the Swedish scientists soon retracted their claims, the priority of the discovery and therefore the naming of the element was disputed between Soviet and American scientists, and it was not until 1997 that International Union of Pure and Applied Chemistry (IUPAC) credited the Soviet team with the discovery, but retained nobelium, the Swedish proposal, as the name of the element due to its long-standing use in the literature.


A graphic depiction of a nuclear fusion reaction
A graphic depiction of a nuclear fusion reaction. Two nuclei fuse into one, emitting a neutron. Reactions that created new elements to this moment were similar, with the only possible difference that several singular neutrons sometimes were released, or none at all.
External video
video iconVisualization of unsuccessful nuclear fusion, based on calculations by the Australian National University[5]

The heaviest[a]atomic nuclei are created in nuclear reactions that combines two other nuclei of unequal size[b] into one; roughly, the more unequal the two nuclei in terms of mass, the greater the possibility that the two react.[11] The material made of the heavier nuclei is made into a target, which is then bombarded by the beam of lighter nuclei. Two nuclei can only fuse into one if they approach each other closely enough; normally, nuclei (all positively charged) repel each other due to electrostatic repulsion. The strong interaction can overcome this repulsion but only within a very short distance from a nucleus; beam nuclei are thus greatly accelerated in order to make such repulsion insignificant compared to the velocity of the beam nucleus.[12] Coming close alone is not enough for two nuclei to fuse: when two nuclei approach each other, they usually remain together for approximately 10-20 seconds and then part ways (not necessarily in the same composition as before the reaction) rather than form a single nucleus.[12][13] If fusion does occur, the temporary merger--termed a compound nucleus--is an excited state. To lose its excitation energy and reach a more stable state, a compound nucleus either fissions or ejects one or several neutrons,[c] which carry away the energy. This occurs in approximately 10-16 seconds after the initial collision.[14][d]

The beam passes through the target and reaches the next chamber, the separator; if a new nucleus is produced, it is carried with this beam.[17] In the separator, the newly produced nucleus is separated from other nuclides (that of the original beam and any other reaction products)[e] and transferred to a surface-barrier detector, which stops the nucleus. The exact location of the upcoming impact on the detector is marked; also marked are its energy and the time of the arrival.[17] The transfer takes about 10-6 seconds; in order to be detected, the nucleus must survive this long.[20] The nucleus is recorded again once its decay is registered, and the location, the energy, and the time of the decay are measured.[17]

Stability of a nucleus is provided by the strong interaction. However, its range is very short; as nuclei become larger, its influence on the outermost nucleons (protons and neutrons) weakens. At the same time, the nucleus is torn apart by electrostatic repulsion between protons, as it has unlimited range.[21] Nuclei of the heaviest elements are thus theoretically predicted[22] and have so far been observed[23] to primarily decay via decay modes that are caused by such repulsion: alpha decay and spontaneous fission;[f] these modes are predominant for nuclei of superheavy elements. Alpha decays are registered by the emitted alpha particles, and the decay products are easy to determine before the actual decay; if such a decay or a series of consecutive decays produces a known nucleus, the original product of a reaction can be determined arithmetically.[g] Spontaneous fission, however, produces various nuclei as products, so the original nuclide cannot be determined from its daughters.[h]

The information available to physicists aiming to synthesize one of the heaviest elements is thus the information collected at the detectors: location, energy, and time of arrival of a particle to the detector, and those of its decay. The physicists analyze this data and seek to conclude that it was indeed caused by a new element and could not have been caused by a different nuclide than the one claimed. Often, provided data is insufficient for a conclusion that a new element was definitely created and there is no other explanation for the observed effects; errors in interpreting data have been made.


The element was named after Alfred Nobel.

The discovery of element 102 was a complicated process and was claimed by groups from Sweden, the United States, and the Soviet Union. The first complete and incontrovertible report of its detection only came in 1966 from the Joint Institute of Nuclear Research at Dubna (then in the Soviet Union).[30]

The first announcement of the discovery of element 102 was announced by physicists at the Nobel Institute in Sweden in 1957. The team reported that they had bombarded a curium target with carbon-13 ions for twenty-five hours in half-hour intervals. Between bombardments, ion-exchange chemistry was performed on the target. Twelve out of the fifty bombardments contained samples emitting (8.5 ± 0.1) MeV alpha particles, which were in drops which eluted earlier than fermium (atomic number Z = 100) and californium (Z = 98). The half-life reported was 10 minutes and was assigned to either 251102 or 253102, although the possibility that the alpha particles observed were from a presumably short-lived mendelevium (Z = 101) isotope created from the electron capture of element 102 was not excluded.[30] The team proposed the name nobelium (No) for the new element,[31][32] which was immediately approved by IUPAC,[33] a decision which the Dubna group characterized in 1968 as being hasty.[34] The following year, scientists at the Lawrence Berkeley National Laboratory repeated the experiment but were unable to find any 8.5 MeV events which were not background effects.[30]

In 1959, the Swedish team attempted to explain the Berkeley team's inability to detect element 102 in 1958, maintaining that they did discover it. However, later work has shown that no nobelium isotopes lighter than 259No (no heavier isotopes could have been produced in the Swedish experiments) with a half-life over 3 minutes exist, and that the Swedish team's results are most likely from thorium-225, which has a half-life of 8 minutes and quickly undergoes triple alpha decay to polonium-213, which has a decay energy of 8.53612 MeV. This hypothesis is lent weight by the fact that thorium-225 can easily be produced in the reaction used and would not be separated out by the chemical methods used. Later work on nobelium also showed that the divalent state is more stable than the trivalent one and hence that the samples emitting the alpha particles could not have contained nobelium, as the divalent nobelium would not have eluted with the other trivalent actinides.[30] Thus, the Swedish team later retracted their claim and associated the activity to background effects.[33]

The Berkeley team, consisting of Albert Ghiorso, Glenn T. Seaborg, John R. Walton and Torbjørn Sikkeland, then claimed the synthesis of element 102 in 1958. The team used the new heavy-ion linear accelerator (HILAC) to bombard a curium target (95% 244Cm and 5% 246Cm) with 13C and 12C ions. They were unable to confirm the 8.5 MeV activity claimed by the Swedes but were instead able to detect decays from fermium-250, supposedly the daughter of 254102 (produced from the curium-246), which had an apparent half-life of ~3 s. Later 1963 Dubna work confirmed that 254102 could be produced in this reaction, but that its half-life was actually . In 1967, the Berkeley team attempted to defend their work, stating that the isotope found was indeed 250Fm but the isotope that the half-life measurements actually related to was californium-244, granddaughter of 252102, produced from the more abundant curium-244. Energy differences were then attributed to "resolution and drift problems", although these had not been previously reported and should also have influenced other results. 1977 experiments showed that 252102 indeed had a 2.3-second half-life. However, 1973 work also showed that the 250Fm recoil could have also easily been produced from the isomeric transition of 250mFm (half-life 1.8 s) which could also have been formed in the reaction at the energy used.[30] Given this, it is probable that no nobelium was actually produced in this experiment.[30]

In 1959, the team continued their studies and claimed that they were able to produce an isotope that decayed predominantly by emission of an 8.3 MeV alpha particle, with a half-life of 3 s with an associated 30% spontaneous fission branch. The activity was initially assigned to 254102 but later changed to 252102. However, they also noted that it was not certain that nobelium had been produced due to difficult conditions.[30] The Berkeley team decided to adopt the proposed name of the Swedish team, "nobelium", for the element.[33]

+ 12
-> 256
-> 252
+ 4 1


Meanwhile, in Dubna, experiments were carried out in 1958 and 1960 aiming to synthesize element 102 as well. The first 1958 experiment bombarded plutonium-239 and -241 with oxygen-16 ions. Some alpha decays with energies just over 8.5 MeV were observed, and they were assigned to 251,252,253102, although the team wrote that formation of isotopes from lead or bismuth impurities (which would not produce nobelium) could not be ruled out. While later 1958 experiments noted that new isotopes could be produced from mercury, thallium, lead, or bismuth impurities, the scientists still stood by their conclusion that element 102 could be produced from this reaction, mentioning a half-life of under 30 seconds and a decay energy of (8.8 ± 0.5) MeV. Later 1960 experiments proved that these were background effects. 1967 experiments also lowered the decay energy to (8.6 ± 0.4) MeV, but both values are too high to possibly match those of 253No or 254No.[30] The Dubna team later stated in 1970 and again in 1987 that these results were not conclusive.[30]

In 1961, Berkeley scientists claimed the discovery of element 103 in the reaction of californium with boron and carbon ions. They claimed the production of the isotope 257103, and also claimed to have synthesized an alpha decaying isotope of element 102 that had a half-life of 15 s and alpha decay energy 8.2 MeV. They assigned this to 255102 without giving a reason for the assignment. The values do not agree with those now known for 255No, although they do agree with those now known for 257No, and while this isotope probably played a part in this experiment, its discovery was inconclusive.[30]

Work on element 102 also continued in Dubna, and in 1964, experiments were carried out there to detect alpha-decay daughters of element 102 isotopes by synthesizing element 102 from the reaction of a uranium-238 target with neon ions. The products were carried along a silver catcher foil and purified chemically, and the isotopes 250Fm and 252Fm were detected. The yield of 252Fm was interpreted as evidence that its parent 256102 was also synthesized: as it was noted that 252Fm could also be produced directly in this reaction by the simultaneous emission of an alpha particle with the excess neutrons, steps were taken to ensure that 252Fm could not go directly to the catcher foil. The half-life detected for 256102 was 8 s, which is much higher than the more modern 1967 value of (3.2 ± 0.2) s.[30] Further experiments were conducted in 1966 for 254102, using the reactions 243Am(15N,4n)254102 and 238U(22Ne,6n)254102, finding a half-life of (50 ± 10) s: at that time the discrepancy between this value and the earlier Berkeley value was not understood, although later work proved that the formation of the isomer 250mFm was less likely in the Dubna experiments than at the Berkeley ones. In hindsight, the Dubna results on 254102 were probably correct and can be now considered a conclusive detection of element 102.[30]

One more very convincing experiment from Dubna was published in 1966, again using the same two reactions, which concluded that 254102 indeed had a half-life much longer than the 3 seconds claimed by Berkeley.[30] Later work in 1967 at Berkeley and 1971 at the Oak Ridge National Laboratory fully confirmed the discovery of element 102 and clarified earlier observations.[33] In December 1966, the Berkeley group repeated the Dubna experiments and fully confirmed them, and used this data to finally assign correctly the isotopes they had previously synthesized but could not yet identify at the time, and thus claimed to have discovered nobelium in 1958 to 1961.[33]

+ 22
-> 260
-> 254
+ 6 1


In 1969, the Dubna team carried out chemical experiments on element 102 and concluded that it behaved as the heavier homologue of ytterbium. The Russian scientists proposed the name joliotium (Jo) for the new element after Irène Joliot-Curie, who had recently died, creating an element naming controversy that would not be resolved for several decades, which each group using its own proposed names.[33]

In 1992, the IUPAC-IUPAP Transfermium Working Group (TWG) reassessed the claims of discovery and concluded that only the Dubna work from 1966 correctly detected and assigned decays to nuclei with atomic number 102 at the time. The Dubna team are therefore officially recognised as the discoverers of nobelium although it is possible that it was detected at Berkeley in 1959.[30] This decision was criticized by Berkeley the following year, calling the reopening of the cases of elements 101 to 103 a "futile waste of time", while Dubna agreed with IUPAC's decision.[34]

In 1994, as part of an attempted resolution to the element naming controversy, IUPAC ratified names for elements 101-109. For element 102, it ratified the name nobelium (No) on the basis that it had become entrenched in the literature over the course of 30 years and that Alfred Nobel should be commemorated in this fashion.[35] Because of outcry over the 1994 names, which mostly did not respect the choices of the discoverers, a comment period ensued, and in 1995 IUPAC named element 102 flerovium (Fl) as part of a new proposal, after either Georgy Flyorov or his eponymous Flerov Laboratory of Nuclear Reactions.[36] This proposal was also not accepted, and in 1997 the name "nobelium" was restored.[35] Today the name "flerovium", with the same symbol, refers to element 114.[37]



Energy required to promote an f electron to the d subshell for the f-block lanthanides and actinides. Above around 210 kJ/mol, this energy is too high to be provided for by the greater crystal energy of the trivalent state and thus einsteinium, fermium, and mendelevium form divalent metals like the lanthanides europium and ytterbium. Nobelium is also expected to form a divalent metal, but this has not yet been confirmed.[38]

In the periodic table, nobelium is located to the right of the actinide mendelevium, to the left of the actinide lawrencium, and below the lanthanide ytterbium. Nobelium metal has not yet been prepared in bulk quantities, and bulk preparation is currently impossible.[39] Nevertheless, a number of predictions and some preliminary experimental results have been done regarding its properties.[39]

The lanthanides and actinides, in the metallic state, can exist as either divalent (such as europium and ytterbium) or trivalent (most other lanthanides) metals. The former have fn+1s2 configurations, whereas the latter have fnd1s2 configurations. In 1975, Johansson and Rosengren examined the measured and predicted values for the cohesive energies (enthalpies of crystallization) of the metallic lanthanides and actinides, both as divalent and trivalent metals.[40][41] The conclusion was that the increased binding energy of the [Rn]5f136d17s2 configuration over the [Rn]5f147s2 configuration for nobelium was not enough to compensate for the energy needed to promote one 5f electron to 6d, as is true also for the very late actinides: thus einsteinium, fermium, mendelevium, and nobelium were expected to be divalent metals, although for nobelium this prediction has not yet been confirmed.[40] The increasing predominance of the divalent state well before the actinide series concludes is attributed to the relativistic stabilization of the 5f electrons, which increases with increasing atomic number: an effect of this is that nobelium is predominantly divalent instead of trivalent, unlike all the other lanthanides and actinides.[42] In 1986, nobelium metal was estimated to have an enthalpy of sublimation between 126 kJ/mol, a value close to the values for einsteinium, fermium, and mendelevium and supporting the theory that nobelium would form a divalent metal.[39] Like the other divalent late actinides (except the once again trivalent lawrencium), metallic nobelium should assume a face-centered cubic crystal structure.[2] Divalent nobelium metal should have a metallic radius of around 197 pm.[39] Nobelium's melting point has been predicted to be 827 °C, the same value as that estimated for the neighboring element mendelevium.[43] Its density is predicted to be around 9.9 ± 0.4 g/cm3.[2]


The chemistry of nobelium is incompletely characterized and is known only in aqueous solution, in which it can take on the +3 or +2 oxidation states, the latter being more stable.[31] It was largely expected before the discovery of nobelium that in solution, it would behave like the other actinides, with the trivalent state being predominant; however, Seaborg predicted in 1949 that the +2 state would also be relatively stable for nobelium, as the No2+ ion would have the ground-state electron configuration [Rn]5f14, including the stable filled 5f14 shell. It took nineteen years before this prediction was confirmed.[44]

In 1967, experiments were conducted to compare nobelium's chemical behavior to that of terbium, californium, and fermium. All four elements were reacted with chlorine and the resulting chlorides were deposited along a tube, along which they were carried by a gas. It was found that the nobelium chloride produced was strongly adsorbed on solid surfaces, proving that it was not very volatile, like the chlorides of the other three investigated elements. However, both NoCl2 and NoCl3 were expected to exhibit nonvolatile behavior and hence this experiment was inconclusive as to what the preferred oxidation state of nobelium was.[44] Determination of nobelium's favoring of the +2 state had to wait until the next year, when cation-exchange chromatography and coprecipitation experiments were carried out on around fifty thousand 255No atoms, finding that it behaved differently from the other actinides and more like the divalent alkaline earth metals. This proved that in aqueous solution, nobelium is most stable in the divalent state when strong oxidizers are absent.[44] Later experimentation in 1974 showed that nobelium eluted with the alkaline earth metals, between Ca2+ and Sr2+.[44] Nobelium is the only known f-block element for which the +2 state is the most common and stable one in aqueous solution. This occurs because of the large energy gap between the 5f and 6d orbitals at the end of the actinide series.[45]

It is expected that the relativistic stabilization of the 7s subshell greatly destabilizes nobelium dihydride, NoH2, and relativistic stabilisation of the 7p1/2 spinor over the 6d3/2 spinor mean that excited states in nobelium atoms have 7s and 7p contribution instead of the expected 6d contribution. The long No-H distances in the NoH2 molecule and the significant charge transfer lead to extreme ionicity with a dipole moment of 5.94 D for this molecule. In this molecule, nobelium is expected to exhibit main-group-like behavior, specifically acting like an alkaline earth metal with its ns2 valence shell configuration and core-like 5f orbitals.[46]

Nobelium's complexing ability with chloride ions is most similar to that of barium, which complexes rather weakly.[44] Its complexing ability with citrate, oxalate, and acetate in an aqueous solution of 0.5 M ammonium nitrate is between that of calcium and strontium, although it is somewhat closer to that of strontium.[44]

The standard reduction potential of the E°(No3+->No2+) couple was estimated in 1967 to be between +1.4 and +1.5 V;[44] it was later found in 2009 to be only about +0.75 V.[47] The positive value shows that No2+ is more stable than No3+ and that No3+ is a good oxidizing agent. While the quoted values for the E°(No2+->No0) and E°(No3+->No0) vary among sources, the accepted standard estimates are -2.61 and -1.26 V.[44] It has been predicted that the value for the E°(No4+->No3+) couple would be +6.5 V.[44] The Gibbs energies of formation for No3+ and No2+ are estimated to be -342 and -480 kJ/mol, respectively.[44]


A nobelium atom has 102 electrons, of which three can act as valence electrons. They are expected to be arranged in the configuration [Rn]5f147s2 (ground state term symbol 1S0), although experimental verification of this electron configuration had not yet been made as of 2006.[39] In forming compounds, all the three valence electrons may be lost, leaving behind a [Rn]5f13 core: this conforms to the trend set by the other actinides with their [Rn]5fn electron configurations in the tripositive state. Nevertheless, it is more likely that only two valence electrons may be lost, leaving behind a stable [Rn]5f14 core with a filled 5f14 shell. The first ionization potential of nobelium was measured to be at most (6.65 ± 0.07) eV in 1974, based on the assumption that the 7s electrons would ionize before the 5f ones;[48] this value has since not yet been refined further due to nobelium's scarcity and high radioactivity.[49] The ionic radius of hexacoordinate and octacoordinate No3+ had been preliminarily estimated in 1978 to be around 90 and 102 pm respectively;[44] the ionic radius of No2+ has been experimentally found to be 100 pm to two significant figures.[39] The enthalpy of hydration of No2+ has been calculated as 1486 kJ/mol.[44]


Twelve isotopes of nobelium are known, with mass numbers 250-260 and 262; all are radioactive.[50] Additionally, nuclear isomers are known for mass numbers 251, 253, and 254.[51][52] Of these, the longest-lived isotope is 259No with a half-life of 58 minutes, and the longest-lived isomer is 251mNo with a half-life of 1.7 seconds.[51][52] However, the still undiscovered isotope 261No is predicted to have a still longer half-life of 170 min.[51][52] Additionally, the shorter-lived 255No (half-life 3.1 minutes) is more often used in chemical experimentation because it can be produced in larger quantities from irradiation of californium-249 with carbon-12 ions.[50] After 259No and 255No, the next most stable nobelium isotopes are 253No (half-life 1.62 minutes), 254No (51 seconds), 257No (25 seconds), 256No (2.91 seconds), and 252No (2.57 seconds).[50][51][52] All of the remaining nobelium isotopes have half-lives that are less than a second, and the shortest-lived known nobelium isotope (250No) has a half-life of only 0.25 milliseconds.[50][51][52] The isotope 254No is especially interesting theoretically as it is in the middle of a series of prolate nuclei from 231Pa to 279Rg, and the formation of its nuclear isomers (of which two are known) is controlled by proton orbitals such as 2f5/2 which come just above the spherical proton shell; it can be synthesized in the reaction of 208Pb with 48Ca.[53]

The half-lives of nobelium isotopes increase smoothly from 250No to 253No. However, a dip appears at 254No, and beyond this the half-lives of even-even nobelium isotopes drop sharply as spontaneous fission becomes the dominant decay mode. For example, the half-life of 256No is almost three seconds, but that of 258No is only 1.2 milliseconds.[50][51][52] This shows that at nobelium, the mutual repulsion of protons poses a limit to the region of long-lived nuclei in the actinide series.[54] The even-odd nobelium isotopes mostly continue to have longer half-lives as their mass numbers increase, with a dip in the trend at 257No.[50][51][52]

Preparation and purification

The isotopes of nobelium are mostly produced by bombarding actinide targets (uranium, plutonium, curium, californium, or einsteinium), with the exception of nobelium-262, which is produced as the daughter of lawrencium-262.[50] The most commonly used isotope, 255No, can be produced from bombarding curium-248 or californium-249 with carbon-12: the latter method is more common. Irradiating a 350 ?g cm-2 target of californium-249 with three trillion (3 × 1012) 73 MeV carbon-12 ions per second for ten minutes can produce around 1200 nobelium-255 atoms.[50]

Once the nobelium-255 is produced, it can be separated out in a similar way as used to purify the neighboring actinide mendelevium. The recoil momentum of the produced nobelium-255 atoms is used to bring them physically far away from the target from which they are produced, bringing them onto a thin foil of metal (usually beryllium, aluminium, platinum, or gold) just behind the target in a vacuum: this is usually combined by trapping the nobelium atoms in a gas atmosphere (frequently helium), and carrying them along with a gas jet from a small opening in the reaction chamber. Using a long capillary tube, and including potassium chloride aerosols in the helium gas, the nobelium atoms can be transported over tens of meters.[55] The thin layer of nobelium collected on the foil can then be removed with dilute acid without completely dissolving the foil.[55] The nobelium can then be isolated by exploiting its tendency to form the divalent state, unlike the other trivalent actinides: under typically used elution conditions (bis-(2-ethylhexyl) phosphoric acid (HDEHP) as stationary organic phase and 0.05 M hydrochloric acid as mobile aqueous phase, or using 3 M hydrochloric acid as an eluant from cation-exchange resin columns), nobelium will pass through the column and elute while the other trivalent actinides remain on the column.[55] However, if a direct "catcher" gold foil is used, the process is complicated by the need to separate out the gold using anion-exchange chromatography before isolating the nobelium by elution from chromatographic extraction columns using HDEHP.[55]


  1. ^ In nuclear physics, an element is called heavy if its atomic number is high; lead (element 82) is one example of such a heavy element. The term "superheavy elements" typically refers to elements with atomic number greater than 103 (although there are other definitions, such as atomic number greater than 100[6] or 112;[7] sometimes, the term is presented an equivalent to the term "transactinide", which puts an upper limit before the beginning of the hypothetical superactinide series).[8] Terms "heavy isotopes" (of a given element) and "heavy nuclei" mean what could be understood in the common language--isotopes of high mass (for the given element) and nuclei of high mass, respectively.
  2. ^ In 2009, a team at JINR led by Oganessian published results of their attempt to create hassium in a symmetric 136Xe + 136Xe reaction. They failed to observe a single atom in such a reaction, putting the upper limit on the cross section, the measure of probability of a nuclear reaction, as 2.5 pb.[9] In comparison, the reaction that resulted in hassium discovery, 208Pb + 58Fe, had a cross section of ~20 pb (more specifically, 19+19
     pb), as estimated by the discoverers.[10]
  3. ^ The greater the excitation energy, the more neutrons are ejected. If the excitation energy is lower than energy binding each neutron to the rest of the nucleus, neutrons are not emitted; instead, the compound nucleus de-excites by emitting a gamma ray.[14]
  4. ^ The definition by the IUPAC/IUPAP Joint Working Party states that a chemical element can only be recognized as discovered if a nucleus of it has not decayed within 10-14 seconds. This value was chosen as an estimate of how long it takes a nucleus to acquire its outer electrons and thus display its chemical properties.[15] This figure also marks the generally accepted upper limit for lifetime of a compound nucleus.[16]
  5. ^ This separation is based on that the resulting nuclei move past the target more slowly then the unreacted beam nuclei. The separator contains electric and magnetic fields whose effects on a moving particle cancel out for a specific velocity of a particle.[18] Such separation can also be aided by a time-of-flight measurement and a recoil energy measurement; a combination of the two may allow to estimate the mass of a nucleus.[19]
  6. ^ Not all decay modes are caused by electrostatic repulsion. For example, beta decay is caused by the weak interaction.[24]
  7. ^ Since mass of a nucleus is not measured directly but is rather calculated from that of another nucleus, such measurement is called indirect. Direct measurements are also possible, but for the most part they have remained unavailable for heaviest nuclei.[25] The first direct measurement of mass of a superheavy nucleus was reported in 2018 at LBNL.[26] Mass was determined from the location of a nucleus after the transfer (the location helps determine its trajectory, which is linked to the mass-to-charge ratio of the nucleus, since the transfer was done in presence of a magnet).[27]
  8. ^ Spontaneous fission was discovered by Soviet physicist Georgy Flerov,[28] a leading scientist at JINR, and thus it was a "hobbyhorse" for the facility.[29] In contrast, the LBL scientists believed fission information was not sufficient for a claim of synthesis of an element. They believed spontaneous fission had not been studied enough to use it for identification of a new element, since there was a difficulty of establishing that a compound nucleus had only ejected neutrons and not charged particles like protons or alpha particles.[16] They thus preferred to link new isotopes to the already known ones by successive alpha decays.[28]


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  4. ^
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