Rutherfordium

Template:Infobox rutherfordium Rutherfordium is a synthetic chemical element; it has symbol Rf and atomic number 104. It is named after physicist Ernest Rutherford. As a synthetic element, it is not found in nature and can only be made in a particle accelerator. It is radioactive; the most stable known isotope, ²⁶⁷Rf, has a half-life of about 48 minutes.

In the periodic table, it is a d-block element and the second of the fourth-row transition elements. It is in period 7 and is a group 4 element. Chemistry experiments have confirmed that rutherfordium behaves as the heavier homolog to hafnium in group 4. The chemical properties of rutherfordium are characterized only partly. They compare well with the other group 4 elements, even though some calculations had indicated that the element might show significantly different properties due to relativistic effects.

In the 1960s, small amounts of rutherfordium were produced at Joint Institute for Nuclear Research in the Soviet Union and at Lawrence Berkeley National Laboratory in California. Priority of discovery and hence the name of the element was disputed between Soviet and American scientists, and it was not until 1997 that the International Union of Pure and Applied Chemistry (IUPAC) established rutherfordium as the official name of the element.

History

Discovery

Rutherfordium was reportedly first detected in 1964 at the Joint Institute for Nuclear Research at Dubna (Soviet Union at the time). Researchers there bombarded a plutonium-242 target with neon-22 ions; a spontaneous fission activity with half-life 0.3 ± 0.1 seconds was detected and assigned to ²⁶⁰104. Later work found no isotope of element 104 with this half-life, so that this assignment must be considered incorrect.

In 1966–1969, the experiment was repeated. This time, the reaction products by gradient thermochromatography after conversion to chlorides by interaction with ZrCl₄. The team identified spontaneous fission activity contained within a volatile chloride portraying eka-hafnium properties.

Template:Nuclide + Template:Nuclide → ^264−x104 → ^264−x104Cl₄

The researchers considered the results to support the 0.3 second half-life. Although it is now known that there is no isotope of element 104 with such a half-life, the chemistry does fit that of element 104, as chloride volatility is much greater in group 4 than in group 3 (or the actinides).

In 1969, researchers at University of California, Berkeley conclusively synthesized the element by bombarding a californium-249 target with carbon-12 ions and measured the alpha decay of ²⁵⁷104, correlated with the daughter decay of nobelium-253:

Template:Nuclide + Template:Nuclide → ²⁵⁷104 + 4 Template:SubatomicParticle

They were unable to confirm the 0.3-second half-life for ²⁶⁰104, and instead found a 10–30 millisecond half-life for this isotope, agreeing with the modern value of 21 milliseconds. In 1970, the American team chemically identified element 104 using the ion-exchange separation method, proving it to be a group 4 element and the heavier homologue of hafnium.

The American synthesis was independently confirmed in 1973 and secured the identification of rutherfordium as the parent by the observation of K-alpha X-rays in the elemental signature of the ²⁵⁷104 decay product, nobelium-253.

Naming controversy

File:Ernest Rutherford2.jpg

Element 104 was eventually named after Ernest Rutherford

File:Igor Kurchatov 001.png

Igor Kurchatov

As a consequence of the initial competing claims of discovery, an element naming controversy arose. Since the Soviets claimed to have first detected the new element they suggested the name kurchatovium (Ku) in honor of Igor Kurchatov (1903–1960), former head of Soviet nuclear research. This name had been used in books of the Soviet Bloc as the official name of the element. The Americans, however, proposed rutherfordium (Rf) for the new element to honor New Zealand physicist Ernest Rutherford, who is known as the "father" of nuclear physics. In 1992, the IUPAC/IUPAP Transfermium Working Group (TWG) assessed the claims of discovery and concluded that both teams provided contemporaneous evidence to the synthesis of element 104 in 1969, and that credit should be shared between the two groups. In particular, this involved the TWG performing a new retrospective reanalysis of the Russian work in the face of the later-discovered fact that there is no 0.3-second isotope of element 104: they reinterpreted the Dubna results as having been caused by a spontaneous fission branch of ²⁵⁹104.

The American group wrote a scathing response to the findings of the TWG, stating that they had given too much emphasis on the results from the Dubna group. In particular they pointed out that the Russian group had altered the details of their claims several times over a period of 20 years, a fact that the Russian team does not deny. They also stressed that the TWG had given too much credence to the chemistry experiments performed by the Russians, considered the TWG's retrospective treatment of the Russian work based on unpublished documents to have been "highly irregular", noted that there was no proof that ²⁵⁹104 had a spontaneous fission branch at all (as of 2021 there still is not),Template:NUBASE2020 and accused the TWG of not having appropriately qualified personnel on the committee. The TWG responded by saying that this was not the case and having assessed each point raised by the American group said that they found no reason to alter their conclusion regarding priority of discovery.

The International Union of Pure and Applied Chemistry (IUPAC) adopted unnilquadium (Unq) as a temporary, systematic element name, derived from the Latin names for digits 1, 0, and 4. In 1994, IUPAC suggested a set of names for elements 104 through 109, in which dubnium (Db) became element 104 and rutherfordium became element 106. This recommendation was criticized by the American scientists for several reasons. Firstly, their suggestions were scrambled: the names rutherfordium and hahnium, originally suggested by Berkeley for elements 104 and 105, were respectively reassigned to elements 106 and 108. Secondly, elements 104 and 105 were given names favored by JINR, despite earlier recognition of LBL as an equal co-discoverer for both of them. Thirdly and most importantly, IUPAC rejected the name seaborgium for element 106, having just approved a rule that an element could not be named after a living person, even though the IUPAC had given the LBNL team the sole credit for its discovery. In 1997, IUPAC renamed elements 104 to 109, and gave elements 104 and 106 the Berkeley proposals rutherfordium and seaborgium. The name dubnium was given to element 105 at the same time. The 1997 names were accepted by researchers and became the standard.

Isotopes

Rutherfordium has no stable or naturally occurring isotopes. Several radioactive isotopes have been synthesized in the laboratory, either by fusing two atoms or by observing the decay of heavier elements. Seventeen different isotopes have been reported with atomic masses from 252 to 270 (with the exceptions of 264 and 269). Most of these decay predominantly through spontaneous fission, particularly isotopes with even neutron numbers, while some of the lighter isotopes with odd neutron numbers also have significant alpha decay branches.

Stability and half-lives

Out of isotopes whose half-lives are known, the lighter isotopes usually have shorter half-lives. The three lightest known isotopes have half-lives of under 50 μs, with the lightest reported isotope ²⁵²Rf having a half-life shorter than one microsecond. The isotopes ²⁵⁶Rf, ²⁵⁸Rf, ²⁶⁰Rf are more stable at around 10 ms; ²⁵⁵Rf, ²⁵⁷Rf, ²⁵⁹Rf, and ²⁶²Rf live between 1 and 5 seconds; and ²⁶¹Rf, ²⁶⁵Rf, and ²⁶³Rf are more stable, at around 1.1, 1.5, and 10 minutes respectively. The most stable known isotope, ²⁶⁷Rf, is one of the heaviest, and has a half-life of about 48 minutes. Rutherfordium isotopes with an odd neutron number tend to have longer half-lives than their even–even neighbors because the odd neutron provides additional hindrance against spontaneous fission.

The lightest isotopes were synthesized by direct fusion between two lighter nuclei and as decay products. The heaviest isotope produced by direct fusion is ²⁶²Rf; heavier isotopes have only been observed as decay products of elements with larger atomic numbers. The heavy isotopes ²⁶⁶Rf and ²⁶⁸Rf have also been reported as electron capture daughters of the dubnium isotopes ²⁶⁶Db and ²⁶⁸Db, but have short half-lives to spontaneous fission. It seems likely that the same is true for ²⁷⁰Rf, a possible daughter of ²⁷⁰Db. These three isotopes remain unconfirmed.

In 1999, American scientists at the University of California, Berkeley, announced that they had succeeded in synthesizing three atoms of ²⁹³Og. These parent nuclei were reported to have successively emitted seven alpha particles to form ²⁶⁵Rf nuclei, but their claim was retracted in 2001. This isotope was later discovered in 2010 as the final product in the decay chain of ²⁸⁵Fl.

Predicted properties

Very few properties of rutherfordium or its compounds have been measured; this is due to its extremely limited and expensive production and the fact that rutherfordium (and its parents) decays very quickly. A few singular chemistry-related properties have been measured, but properties of rutherfordium metal remain unknown and only predictions are available.

Chemical

Rutherfordium is the first transactinide element and the second member of the 6d series of transition metals. Calculations on its ionization potentials, atomic radius, as well as radii, orbital energies, and ground levels of its ionized states are similar to that of hafnium and very different from that of lead. Therefore, it was concluded that rutherfordium's basic properties will resemble those of other group 4 elements, below titanium, zirconium, and hafnium. Some of its properties were determined by gas-phase experiments and aqueous chemistry. The oxidation state +4 is the only stable state for the latter two elements and therefore rutherfordium should also exhibit a stable +4 state. In addition, rutherfordium is also expected to be able to form a less stable +3 state. The standard reduction potential of the Rf⁴⁺/Rf couple is predicted to be higher than −1.7 V.Template:Fricke1975

Initial predictions of the chemical properties of rutherfordium were based on calculations which indicated that the relativistic effects on the electron shell might be strong enough that the 7p orbitals would have a lower energy level than the 6d orbitals, giving it a valence electron configuration of 6d¹ 7s² 7p¹ or even 7s² 7p², therefore making the element behave more like lead than hafnium. With better calculation methods and experimental studies of the chemical properties of rutherfordium compounds it could be shown that this does not happen and that rutherfordium instead behaves like the rest of the group 4 elements. Later it was shown in ab initio calculations with the high level of accuracy that the Rf atom has the ground state with the 6d² 7s² valence configuration and the low-lying excited 6d¹ 7s² 7p¹ state with the excitation energy of only 0.3–0.5 eV.

In an analogous manner to zirconium and hafnium, rutherfordium is projected to form a very stable, refractory oxide, RfO₂. It reacts with halogens to form tetrahalides, RfX₄, which hydrolyze on contact with water to form oxyhalides RfOX₂. The tetrahalides are volatile solids existing as monomeric tetrahedral molecules in the vapor phase.

In the aqueous phase, the Rf⁴⁺ ion hydrolyzes less than titanium(IV) and to a similar extent as zirconium and hafnium, thus resulting in the RfO²⁺ ion. Treatment of the halides with halide ions promotes the formation of complex ions. The use of chloride and bromide ions produces the hexahalide complexes Template:Chem and Template:Chem. For the fluoride complexes, zirconium and hafnium tend to form hepta- and octa- complexes. Thus, for the larger rutherfordium ion, the complexes Template:Chem, Template:Chem and Template:Chem are possible.

Physical and atomic

Rutherfordium is expected to be a solid under normal conditions and have a hexagonal close-packed crystal structure (^c/_a = 1.61), similar to its lighter congener hafnium. It should be a metal with density ~17 g/cm³. The atomic radius of rutherfordium is expected to be ~150 pm. Due to relativistic stabilization of the 7s orbital and destabilization of the 6d orbital, Rf⁺ and Rf²⁺ ions are predicted to give up 6d electrons instead of 7s electrons, which is the opposite of the behavior of its lighter homologs. When under high pressure (variously calculated as 72 or ~50 GPa), rutherfordium is expected to transition to body-centered cubic crystal structure; hafnium transforms to this structure at 71±1 GPa, but has an intermediate ω structure that it transforms to at 38±8 GPa that should be lacking for rutherfordium.

Experimental chemistry

Gas phase

File:RfCl4.png

The tetrahedral structure of the RfCl₄ molecule

Early work on the study of the chemistry of rutherfordium focused on gas thermochromatography and measurement of relative deposition temperature adsorption curves. The initial work was carried out at Dubna in an attempt to reaffirm their discovery of the element. Recent work is more reliable regarding the identification of the parent rutherfordium radioisotopes. The isotope ^261mRf has been used for these studies, though the long-lived isotope ²⁶⁷Rf (produced in the decay chain of ²⁹¹Lv, ²⁸⁷Fl, and ²⁸³Cn) may be advantageous for future experiments. The experiments relied on the expectation that rutherfordium would be a 6d element in group 4 and should therefore form a volatile molecular tetrachloride, that would be tetrahedral in shape. Rutherfordium(IV) chloride is more volatile than its lighter homologue hafnium(IV) chloride (HfCl₄) because its bonds are more covalent.

A series of experiments confirmed that rutherfordium behaves as a typical member of group 4, forming a tetravalent chloride (RfCl₄) and bromide (RfBr₄) as well as an oxychloride (RfOCl₂). A decreased volatility was observed for Template:Chem when potassium chloride is provided as the solid phase instead of gas, highly indicative of the formation of nonvolatile Template:Chem mixed salt.

Aqueous phase

Rutherfordium is expected to have the electron configuration [Rn]5f¹⁴ 6d² 7s² and therefore behave as the heavier homologue of hafnium in group 4 of the periodic table. It should therefore readily form a hydrated Rf⁴⁺ ion in strong acid solution and should readily form complexes in hydrochloric acid, hydrobromic or hydrofluoric acid solutions.

The most conclusive aqueous chemistry studies of rutherfordium have been performed by the Japanese team at Japan Atomic Energy Research Institute using the isotope ^261mRf. Extraction experiments from hydrochloric acid solutions using isotopes of rutherfordium, hafnium, zirconium, as well as the pseudo-group 4 element thorium have proved a non-actinide behavior for rutherfordium. A comparison with its lighter homologues placed rutherfordium firmly in group 4 and indicated the formation of a hexachlororutherfordate complex in chloride solutions, in a manner similar to hafnium and zirconium.

Template:Chem + 6 Template:Chem → Template:Chem

Very similar results were observed in hydrofluoric acid solutions. Differences in the extraction curves were interpreted as a weaker affinity for fluoride ion and the formation of the hexafluororutherfordate ion, whereas hafnium and zirconium ions complex seven or eight fluoride ions at the concentrations used:

Template:Chem + 6 Template:Chem → Template:Chem

Experiments performed in mixed sulfuric and nitric acid solutions shows that rutherfordium has a much weaker affinity towards forming sulfate complexes than hafnium. This result is in agreement with predictions, which expect rutherfordium complexes to be less stable than those of zirconium and hafnium because of a smaller ionic contribution to the bonding. This arises because rutherfordium has a larger ionic radius (76 pm) than zirconium (71 pm) and hafnium (72 pm), and also because of relativistic stabilisation of the 7s orbital and destabilisation and spin–orbit splitting of the 6d orbitals.

Coprecipitation experiments performed in 2021 studied rutherfordium's behaviour in basic solution containing ammonia or sodium hydroxide, using zirconium, hafnium, and thorium as comparisons. It was found that rutherfordium does not strongly coordinate with ammonia and instead coprecipitates out as a hydroxide, which is probably Rf(OH)₄.

External links

• Template:Commons category-inline
• Rutherfordium at The Periodic Table of Videos (University of Nottingham)
• WebElements.com – Rutherfordium