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Nuclear Data Sheets for A = 89

The evaluated experimental data are presented for 14 known nuclides of mass 89 (Ge, As, Se, Br, Kr, Rb, Sr, Y, Zr, Nb, Mo, Tc, Ru, Rh). New data on high–spin excitations are available for {sup 89}Kr, {sup 89}Rb, {sup 89}Sr, {sup 89}Tc and {sup 89}Ru, including a superdeformed structure in {sup 89}Tc. Fluorescence studies in {sup 89}Y have revealed a large number of new levels in 7–11 MeV range. New two–neutron transfer data are available for {sup 89}Zr. New direct and precise measurement of atomic masses of {sup 89}Se, {sup 89}Br, 89{sup K}r, {sup 89}Rb, {sup 89}Mo and {sup 89}Tc have greatly improved the Q value landscape in this mass region. This work supersedes previous A=89 evaluation published in 1998Si31, and also the older ones 1989Si20, 1975Ko21, and M.W. Johns et al., Nuclear Data Tables A 8, 373 (1970). In spite of extensive experimental work on the isobaric nuclei of this mass chain several deficiencies remain. The identification of {sup 89}Rh isotope remains unconfirmed. The half–lives of ground states of {sup 89}Ge, {sup 89}As and {sup 89}Rh have not been measured, only the lower limits are estimated from time–of–flight in a reaction and experimental arrangement, where produced and identified. The decay schemes of {sup 89}Ge, {sup 89}As, {sup 89}Se, {sup 89}Ru and {sup 89}Rh are not known, and those for {sup 89}Tc and {sup 89}Mo are incomplete. High–lying (neutron unbound) levels in {sup 89}Kr, expected to be populated in the decay of {sup 89}Br, have not been investigated. The spins and parities for levels in {sup 89}Kr are largely unassigned, while for {sup 89}Tc and {sup 89}Ru, only few low–spin excitations are established. For {sup 89}Rb, little information is available for high–spin structures. Detailed gamma–ray data are available for {sup 88}Sr(n,γ){sup 89}Sr reaction, but most of these γ rays remain unassigned in a level scheme. Excited state data are nonexistent for {sup 89}Ge, {sup 89}As, {sup 89}Se, {sup 89}Br and {sup 89}Rh. The {sup 89}Y and {sup 89}Zr are the most extensively studied nuclei in A=89.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Improved Cumulative Fission Yield Measurements with Fission Spectrum Neutrons on 235 U

Two isotopically-characterized targets of high-purity (99.84±0.03%) 235 U-oxide and a neutron dosimetry package were exposed to a pulsed neutron irradiation using the Godiva critical assembly at the National Criticality Experiments Research Center. Following irradiation, the fissioned targets were counted with a broad-energy germanium detector. Estimates of the total fissions for each target were made using measurements of well-known fission products. The total fission values were then used to measure the fission yields of 21 fission products with half-lives between 636 and 119,700 seconds. Mean values of seventeen of the measured fission products fell within the 95% confidence level of the Evaluated Nuclear Data Files VII.1/b (ENDF/B-VII.1) using the larger of the two uncertainties: 84g Br, 89 Rb, 91 Sr, 93 Y, 97 Zr, 101 Mo, 105 Ru, 128 Sn, 129 Sb, 130g Sb, 131 Sb, 131m Te, 133 I, 135 I, 141 Ba, 142 Ba, and 142 La. Seven isotopes were measured to better precision than is listed in the ENDF/B-VII.1 database: 89 Rb, 93 Y, 128 Sn, 129 Sb, 130g Sb, 131m Te, and 133 I. Four of the measured isotopes were found to be statistically different from the ENDF/B-VII.1 database: 94 Y, 134 Te, 134 I, and 138 Xe. Two of the isotopic analyses conducted in this paper fit the parent and daughter data simultaneously. The parent-daughter pairs measured in this way were the 134 Te/I and 142 Ba/La pairs. The fission yield results obtained in this way are unique, especially for 134 I, because the parent and daughter half-lives are so close. Here, given the limited number of direct measurements of the 134 Te/I pair from fast neutron induced fission and the seemingly high estimate for 134 Te from previous work, it is likely that the value in this paper is more accurate; however, additional measurements of this pair are needed to validate this assertion.

42 ENGINEERING↗

The series of carbon-chain complexes {Ru(dppe)Cp*}₂{μ-(C≡C )x } (x = 4–8, 11): Synthesis, structures, properties and some reactions

The construction of a series of compounds {Ru(dppe)Cp*} 2 (μ-C 2x ) (Ru*-C2x-Ru*, x = 4–8, 11)) is described. A direct reaction between RuCl(dppe)Cp* and Me 3 Si(Ctriple bond; length of mdashC) 4 SiMe 3 afforded Ru*-C8-Ru* in 89% yield. The Pd(0)/Cu(I)-catalysed coupling of Ru{Ctriple bond; length of mdashCCtriple bond; length of mdashCAu(PPh 3 )}(dppe)Cp*Ru*-C4-Au (2 equiv.) with diiodoethyne gave Ru*-C10-Ru* (64%), or of 1 equiv. with I(Ctriple bond; length of mdashC) 3 I gave Ru*-C14-Ru* (36%); similarly, Ru{(Ctriple bond; length of mdashC) 4 Au(PPh 3 )}(dppe)Cp*Ru*-C8-Au and I(Ctriple bond; length of mdashC) 3 I gave Ru*-C22-Ru* (12%). Desilylation (TBAF) of Ru{(Ctriple bond; length of mdashC)xSiMe 3 }(dppe)Cp*Ru*-C2x-Si (x = 3, 4) followed by oxidative coupling [Cu(OAc) 2 /py] gave Ru*-C12-Ru* (82%) and Ru*-C16-Ru* (58%), respectively. Similar oxidative coupling of Ru(Ctriple bond; length of mdashCCtriple bond; length of mdashCH)(dppe)Cp* was a second route to Ru*-C8-Ru* (82%). Appropriate precursors are already known, or obtained by coupling of Ru*-C2x-Si (x = 2, 4) with AuCl(PPh 3 )/NaOMe [Ru*-C4-Au, 95%; Ru*-C8-Au, 74%] or from Pd(0)/Cu(I) catalysed coupling of Ru*-C2x-Au (x = 2, 3) with I(Ctriple bond; length of mdashC) 2 SiMe 3 (Ru*-C8-Si, 64%; Ru*-C10-Si, 2%). Reactions between Ru*-C2x-Ru* (x = 3, 4) and Fe 2 (CO) 9 gave {Fe 3 (CO) 9 }{μ 3 -CCtriple bond; length of mdashC[Ru(dppe)Cp*]} 2 Fe(C 3 -Ru*) 2 and {Fe 3 (CO) 9 }{μ 3 -CCtriple bond; length of mdashC[Ru(dppe)Cp*]}{μ 3 -C(Ctriple bond; length of mdashC) 2 [Ru(dppe)Cp*]} Fe(C 3 -Ru*)(C 5 -Ru*), respectively. The redox properties of the series of complexes with 2x = 2–16 were measured and showed a diminution of the separation of the first two oxidation potentials, ΔE = E 2 - E 1 , with increasing carbon chain length. The X-ray-determined molecular structures of Ru*-C8-Si, Ru*-C8-Ru*, Ru*-C14-Ru* (two C 6 H 6 solvates), {Ru(PPh 3 ) 2 Cp} 2 {μ-(Ctriple bond; length of mdashC) 4 }·4CHCl 3 Ru-C 8 -Ru·4CHCl 3 and of Fe(C 3 -Ru*) 2 and Fe(C 3 -Ru*)(C 5 -Ru*) are reported.

carbon-chain↗