Rutherfordium (Rf)
transition-metalSolid
Standardatomgewicht
263 uElektronenkonfiguration
[Rn] 7s2 5f14 6d2Schmelzpunkt
2126,85 °CSiedepunkt
5526,85 °CDichte
2,33e+4 kg/m³Oxidationszustände
+3, +4Elektronegativität (Pauling)
N/AIonisierungsenergie (1.)
6,02 eVEntdeckungsjahr
1964Atomradius
150 pmDetails
Rutherfordium is a synthetic transactinide element and the first member of the 6d transition-metal series. All confirmed isotopes are radioactive and short-lived, so its chemistry is studied atom by atom. Chemical experiments show behavior broadly consistent with a group 4 element, analogous to hafnium and zirconium, with the +4 oxidation state dominant in aqueous and halide systems. Relativistic effects and nuclear instability make direct measurements difficult.
Rutherfordium does not occur naturally in the Earth’s crust. Credit for the first synthesis of this element is given jointly to Albert Ghiorso and his team at the University of California in Berkeley and Georgi Flerov and his team at the Joint Institute for Nuclear Research (JINR) in Dubna, Russia. The element is named for Ernest Rutherford (Fig. IUPAC.104.1), who won the Nobel Prize for developing the theory of radioactive transformations [645].
Rutherfordium is of interest in particle physics research, but it has no commercial applications. 261Rf was one of the decay products used to confirm the synthesis of copernicium in a particle accelerator experiment [634].
Rutherfordium named after Ernest Rutherford.
Scientists working at the Joint Institute for Nuclear Research in Dubna, Russia, first reported the production of rutherfordium in 1964. They bombarded atoms of plutonium-242 with ions of neon-22, forming what they believed to be atoms of rutherfordium-260 and four free neutrons. In 1969, a group of scientists working at the Lawrence Radiation Laboratory, now known as the Lawrence Berkeley Laboratory, in Berkeley, California, attempted to confirm the Dubna group's discovery. Lacking the equipment needed to accelerate neon ions, the Berkeley group, led by Albert Ghiorso, bombarded atoms of californium-248 and californium-249 with ions of carbon-12 and carbon-13, producing atoms of rutherfordium-257, rutherfordium-258, rutherfordium-259 and rutherfordium-261. They were, however, unable to produce the same isotope as the Dubna group. Credit for the discovery of rutherfordium is still under debate. Rutherfordium's most stable isotope, rutherfordium-263, has a half-life of about 10 minutes and decays through spontaneous fission.
In 1964, workers at the Joint Nuclear Research Institute at Dubna (U.S.S.R.) bombarded plutonium with accelerated 113 to 115 MeV neon ions. By measuring fission tracks in a special glass with a microscope, they detected an isotope that decays by spontaneous fission. They suggested that this isotope, which had a half-life of 0.3 +/- 0.1 s might be 260-104, produced by the following reaction: 242Pu + 22Ne >260Rf +4n.
Element 104, the first transactinide element, is expected to have chemical properties similar to those of hafnium. It would, for example, form a relatively volatile compound with chlorine (a tetrachloride).
The Soviet scientists have performed experiments aimed at chemical identification, and have attempted to show that the 0.3-s activity is more volatile than that of the relatively nonvolatile actinide trichlorides. This experiment does not fulfill the test of chemically separating the new element from all others, but it provides important evidence for evaluation. Data issued by Soviet scientists reduced the half-life of the isotope they worked with from 0.3 to 0.15 s.
No macroscopic sample of rutherfordium has been prepared, and its visible appearance is unknown. Calculations generally treat it as a very heavy metallic solid under ordinary conditions, but this remains a prediction rather than an observed bulk property.
Rutherfordium has no practical use outside scientific research. It is produced in accelerator experiments to study the limits of the periodic table, transactinide nuclear stability, and the chemistry of single atoms. Individual isotopes have been used in decay-chain identification and in rapid chemical separations designed to compare group 4 behavior with zirconium and hafnium. There is no medical, industrial, structural, or consumer application for the element.
Due to the small amounts produced and its short half-life, there are currently no uses for rutherfordium outside of basic scientific research.
Rutherfordium chemistry has been inferred from very small numbers of atoms in fast gas-phase and aqueous experiments. The most important oxidation state is +4, matching its placement below hafnium. Volatile tetrachloride behavior has been studied for rutherfordium tetrachloride, RfCl₄, in comparison with zirconium tetrachloride, ZrCl₄, and hafnium tetrachloride, HfCl₄. In aqueous solution, hydrolysis, fluoride complexation, and chloride complexation indicate a hard, highly charged cation with group 4 character, although relativistic effects can alter detailed complex stability.
See more information at the Rutherfordium compound page.
The safety concern is radiological rather than chemical toxicity in ordinary handling, because only atom-scale quantities are produced. Hazards depend on the isotope and its decay products; many known isotopes decay by alpha emission, spontaneous fission, or both. Accelerator targets, collection systems, and contaminated apparatus require radiological controls, but rutherfordium itself is not encountered by the public or in commerce.
Rutherfordium has no confirmed natural environmental occurrence. Any atoms made in laboratories decay rapidly and are produced in quantities far too small to form an environmental reservoir or chemical cycle. Its environmental behavior as a bulk substance is therefore unobserved; only its predicted or atom-at-a-time chemical interactions can be compared with those of other group 4 metals.
Rutherfordium has no commodity market, no stockpiled supply, and no economic demand. Production requires heavy-ion accelerators, specialized targets, and rapid detection systems, yielding atoms or very small numbers of atoms for immediate study. Isotopes are made by nuclear reactions such as bombarding actinide targets with lighter ions, and the practical constraint is experimental access rather than raw-material value. Recycling and substitution are not relevant except in the general sense that other elements are used whenever a stable material is needed.
Made by bombarding californium-249 with beams of carbon-12 and 13, which produced an isotope with half lives of 4+ and 3 sec.
Rutherfordium is not expected to be a persistent cosmic element. Its known isotopes have half-lives far too short for primordial survival, and any atoms formed in extreme astrophysical nucleosynthesis would decay quickly into lighter nuclei. No extraterrestrial reservoir is known, and its significance in the universe is chiefly as a laboratory probe of very heavy nuclei.
- Rutherfordium was central to early naming disputes over the first transactinide elements.
- Its chemistry must often be completed before the atom decays.
- Gas-phase studies have compared RfCl₄ with the tetrachlorides of zirconium and hafnium.
- Some rutherfordium isotopes are identified through linked alpha-decay chains.
- The element is named for Ernest Rutherford.
Bilder
Eigenschaften
Physikalisch
- Atomradius (empirisch)
- 150 pm Vergleiche Atomradius (empirisch) aller Elemente →
- Dichte
- 2,33 × 104 kg/m³ Vergleiche Dichte aller Elemente →
- Aggregatzustand bei Standardbedingungen
- Fest Vergleiche Aggregatzustand bei Standardbedingungen aller Elemente →
- Schmelzpunkt
- 2126,85 °C Vergleiche Schmelzpunkt aller Elemente →
- Siedepunkt
- 5526,85 °C Vergleiche Siedepunkt aller Elemente →
Chemisch
- Elektronenaffinität
- 0,65 eV
- Ionisierungsenergie (1.)
- 6,02 eV Vergleiche Ionisierungsenergie (1.) aller Elemente →
- Ionisierungsenergie (2.)
- 14,350049 eV Vergleiche Ionisierungsenergie (2.) aller Elemente →
- Ionisierungsenergie (3.)
- 23,840082 eV Vergleiche Ionisierungsenergie (3.) aller Elemente →
- Ionisierungsenergie (4.)
- 31,87011 eV Vergleiche Ionisierungsenergie (4.) aller Elemente →
- Ionisierungsenergie (5.)
- 64,00022 eV Vergleiche Ionisierungsenergie (5.) aller Elemente →
- Oxidationszustände
- +3, +4 Vergleiche Oxidationszustände aller Elemente →
- Valenzelektronen
- 4 Vergleiche Valenzelektronen aller Elemente →
- Elektronenkonfiguration
- [Rn] 7s2 5f14 6d2
Thermodynamisch
N/A
Nuklear
- Protonen
- 104 Vergleiche Protonen aller Elemente →
- Neutronen
- 162 Vergleiche Neutronen aller Elemente →
- Bekannte Isotope
- 16 Vergleiche Bekannte Isotope aller Elemente →
- Stabile Isotope
- 0 Vergleiche Stabile Isotope aller Elemente →
- Massenzahl (stabilstes)
- 267
- Stabilstes Isotop
- Rf-266
- Entdeckungsjahr
- 1964
Häufigkeit
N/A
Kristallstruktur
N/A
Elektronische Struktur
- Elektronen pro Schale
- 2, 8, 18, 32, 32, 10, 2 Vergleiche Elektronen pro Schale aller Elemente →
Identifikatoren
- CAS-Nummer
- 53850-36-5 Vergleiche CAS-Nummer aller Elemente →
- Termsymbol
- 3F2
- InChI
- InChI=1S/Rf
- InChI-Key
- YGPLJIIQQIDVFJ-UHFFFAOYSA-N
Elektronenkonfiguration Vorhergesagt
Rf: 5f¹⁴ 6d² 7s²[Rn] 5f¹⁴ 6d² 7s²1s² 2s² 2p⁶ 3s² 3p⁶ 3d¹⁰ 4s² 4p⁶ 4d¹⁰ 5s² 5p⁶ 4f¹⁴ 5d¹⁰ 6s² 6p⁶ 5f¹⁴ 6d² 7s²Atommodell
Isotope ändern die Neutronenzahl, Masse und Stabilität — nicht die Elektronenkonfiguration eines neutralen Atoms.
Schematisches Atommodell, nicht maßstabsgetreu.
Atomarer Fingerabdruck
Emissions- / Absorptionsspektrum
Isotopenverteilung
Keine stabilen Isotope.
| Massenzahl | Atommasse (u) | Natürliche Häufigkeit | Halbwertszeit |
|---|---|---|---|
| 262 Radioaktiv | 262,10992 ± 0,00024 | N/A | 250 ms |
| 254 Radioaktiv | 254,10005 ± 0,0003 | N/A | 22.9 us |
| 260 Radioaktiv | 260,10644 ± 0,00022 | N/A | 21 ms |
| 253 Radioaktiv | 253,10044 ± 0,00044 | N/A | 13 ms |
| 258 Radioaktiv | 258,103428 ± 0,000034 | N/A | 12.5 ms |
Phase / Zustand
Grund: 2101,8 °C unter Schmelzpunkt (2126,85 °C)
Schematisch, nicht maßstabsgetreu
Phasenübergangspunkte
Dichte
Bei Standardbedingungen
Bei Standardbedingungen
Atomspektren
10 von 93 angezeigt. Sortiert nach Ionenladung (aufsteigend).
Niveaudaten ?
| Ion | Ladung | Niveaus |
|---|---|---|
| Rf I | 0 | 2 |
| Rf II | +1 | 2 |
| Rf III | +2 | 2 |
| Rf IV | +3 | 2 |
| Rf V | +4 | 2 |
| Rf VI | +5 | 2 |
| Rf VII | +6 | 2 |
| Rf VIII | +7 | 2 |
| Rf IX | +8 | 2 |
| Rf X | +9 | 2 |
Kristallstrukturdaten nicht verfügbar
Verbindungen
Isotope (5)
In 1969 Ghiorso, Nurmia, Harris, K.A.Y. Eskola, and P.L. Eskola of the University of California at Berkeley reported that they had positively identified two, and possibly three isotopes of Element 104. The group indicated that, after repeated attempts, they produced isotope 260104 reported by the Dubna groups in 1964.
| Massenzahl | Atommasse (u) | Natürliche Häufigkeit | Halbwertszeit | Zerfallsart | |
|---|---|---|---|---|---|
| 262 Radioaktiv | 262,10992 ± 0,00024 | N/A | 250 ms | SF ≈100% | |
| 254 Radioaktiv | 254,10005 ± 0,0003 | N/A | 22.9 us | SF ≈100%α<1.5% | |
| 260 Radioaktiv | 260,10644 ± 0,00022 | N/A | 21 ms | SF ≈100%α ?β+ ? | |
| 253 Radioaktiv | 253,10044 ± 0,00044 | N/A | 13 ms | SF ≈100%α ? | |
| 258 Radioaktiv | 258,103428 ± 0,000034 | N/A | 12.5 ms | SF =95.1±1.6%α =4.9±1.6% |
Erweiterte Eigenschaften
Kovalente Radien (Erweitert)
- Kovalenzradius (Pyykkö)
- 157 pm
- Kovalenzradius (Pyykkö, doppelt)
- 140 pm
- Kovalenzradius (Pyykkö, dreifach)
- 131 pm
Nummerierungsskalen
- Mendeleev
- 46
Polarisierbarkeit & Dispersion
- Dipolpolarisierbarkeit
- 112 a.u.
- Dipolpolarisierbarkeit (Uns.)
- 10 a.u.
Oxidationszustands-Kategorien
Erweiterte Referenzdaten
Isotopenzerfallsarten (33)
| Isotop | Modus | Intensität |
|---|---|---|
| 253 | SF | 100% |
| 253 | A | — |
| 254 | SF | 100% |
| 254 | A | 1,5% |
| 255 | A | 52,8% |
| 255 | SF | 47,2% |
| 255 | B+ | 6% |
| 256 | SF | 99,7% |
| 256 | A | 0,3% |
| 257 | A | 89,3% |
Zusätzliche Daten
Estimated Crustal Abundance
The estimated element abundance in the earth's crust.
Not Applicable
Referenzen (1)
- [5] Rutherfordium https://education.jlab.org/itselemental/ele104.html
Estimated Oceanic Abundance
The estimated element abundance in the earth's oceans.
Not Applicable
Referenzen (1)
- [5] Rutherfordium https://education.jlab.org/itselemental/ele104.html
Referenzen
(8)
Data deposited in or computed by PubChem
The half-life and atomic mass data was provided by the Atomic Mass Data Center at the International Atomic Energy Agency.
Element data are cited from the Atomic weights of the elements (an IUPAC Technical Report). The IUPAC periodic table of elements can be found at https://iupac.org/what-we-do/periodic-table-of-elements/. Additional information can be found within IUPAC publication doi:10.1515/pac-2015-0703 Copyright © 2020 International Union of Pure and Applied Chemistry.
The information are cited from Pure Appl. Chem. 2018; 90(12): 1833-2092, https://doi.org/10.1515/pac-2015-0703.
Thomas Jefferson National Accelerator Facility (Jefferson Lab) is one of 17 national laboratories funded by the U.S. Department of Energy. The lab's primary mission is to conduct basic research of the atom's nucleus using the lab's unique particle accelerator, known as the Continuous Electron Beam Accelerator Facility (CEBAF). For more information visit https://www.jlab.org/
The periodic table at the LANL (Los Alamos National Laboratory) contains basic element information together with the history, source, properties, use, handling and more. The provenance data may be found from the link under the source name.
The periodic table contains NIST's critically-evaluated data on atomic properties of the elements. The provenance data that include data for atomic spectroscopy, X-ray and gamma ray, radiation dosimetry, nuclear physics, and condensed matter physics may be found from the link under the source name. Ref: https://www.nist.gov/pml/atomic-spectra-database
This section provides all form of data related to element Rutherfordium.
