The spectrum of HeAr+

Two band groups near 1450 Å, first observed by Tanaka, Yoshino, and Freeman (J. Chem. Phys.62, 4484–4496 (1975)) in discharges through mixtures of helium and argon and assigned by them to the HeAr⁺ ion, were studied under high resolution. Like the similar spectrum of HeNe⁺ previously investigated, the spectrum of HeAr⁺ is a charge transfer spectrum. The upper state B²Σ⁺ of both band groups is derived from $\text{He}{}^{\mathrm{+}}\text{(}{}^2\text{S) +}\text{Ar}\text{(}{}^1\text{S)}$ while the two lower states $\text{A}{}_2{}^2\text{Π}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$ and X²Σ⁺ are derived from $\text{He}\text{(}{}^1\text{S) +}\text{Ar}{}^{\mathrm{+}}\text{(}{}^2\text{P)}$. All three states are very weakly bound, the two lower states even more weakly than the upper state. Unlike HeNe⁺ most of the HeAr⁺ bands are violet shaded. In the longward band group each band shows only three branches while in the shortward group there are four. The former observation shows that the $\text{A}{}_2{}^2\text{Π}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$ state behaves like a ²Σ^? state with γ_v ≈ 0. The B, D, γ, p, and ΔG values of all states were evaluated. While the B_v values of upper and lower states are nearly equal, the D_v values are quite different and this difference accounts for the violet shading of most of the bands even when B′_v is slightly smaller than B″_v; it also accounts for some of the extraheads and linelike features in the rotational structure. As in HeNe⁺ the ${}^2\text{Π}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$ component of ²Π was not observed.     

Medium-spin levels and the character of the 20.4 ns 132+ isomer in 145Gd

Levels of the N = 81 nucleus ¹⁴⁵Gd have been investigated by in-beam γ-ray and conversion electron spectroscopy with the ¹⁴⁴Sm(³He, 2n) reaction. Fourteen new low- and medium-spin states between 1.0 and 2.4 MeV excitation, the known yrast levels up to spin $\text{21}\text{2}{}^{\mathrm{+}}$, five other high-spin non-yrast states and a new 20.4 ns $\text{13}\text{2}$ isomer at 2200.2 keV in ¹⁴⁵Gd have been observed. The isomer decays via a fast 927.3 keV E3 transition with B(E3) = 48 ± 7 W.u. Another weaker decay branch is a mixed, strongly hindered E1 + M2 + E3 transition to the $\text{v}\text{h}{}^{\mathrm{?1}}{}_{\mathrm{<mtext>11</mtext><mtext>2</mtext>}}$ state. We propose an octupole $\text{v}\text{f}{}_{\mathrm{<mtext>7</mtext><mtext>2</mtext>}}\text{j}{}^{\mathrm{?2}}\text{× 3}{}^{\mathrm{?}}$ main configuration for the isomer, analogous to the 997 keV $\text{13}\text{2}{}^{\mathrm{+}}$ isomer in ¹⁴⁷Gd. The levels of ¹⁴⁵Gd are discussed on the basis of the spherical shell model.     

The magnetic rotation spectrum of iodine monobromide

The MRS of IBr in the visible region of the spectrum has been studied at high resolution and a rotational and vibrational analysis is reported. The spectrum consists of short runs in J′ for several neighboring vibrational states of the mixed B, ${}^3\text{Π}{}_0{}^{\mathrm{+}}$, and $\text{B}\text{?}\text{′}$, 0⁺ electronic states. These results imply that only a small number of closely related rotational-vibrational states of the combined system have sufficiently long lifetimes to provide the sharp lines required for the appearance of a MRS. The values observed extend to higher energies similar results reported by Selin for the absorption spectrum.     

Energy levels of low lying triplet states of N2 from infrared emission studies

A theoretical model used to describe the $\text{B′}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}$ and B³Π_g states of N₂ is presented. Using recently acquired high resolution spectra of the $\text{B′}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}\text{→ B}{}^3\text{Π}{}_{\mathrm{g}}$ (0-0) band, rotational energy levels of the v = 0 vibrational levels of these two states are generated with this model. These levels are in excellent agreement with those obtained using a combination differences technique. The precision of the model generated levels is 0.01 cm^?1. The previously unpublished rotational levels of Dieke and Heath for the $\text{A}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$, B³Π_g and C³Π_u states are referenced to the $\text{N}{}_2\text{X}{}^1\text{Σ}{}_{\mathrm{g}}{}^{\mathrm{+}}$ (v = 0, J = 0) ground level and tabulated here. Estimates of the precision of their work are made.     

The decay process 11ΛB → π− + 11C

The branching ratios are calculated for ¹¹_ΛB decay to the ¹¹C ground and excited states below 8 MeV for two possible spin values of ¹¹_ΛB. It is found that the decay rate to the ¹¹C^★ state at E^★ = 6.48 MeV is comparable in magnitude to that leading to the ¹¹C ground state if $\text{J(}{}^{11}{}_{\mathrm{\Lambda }}\text{B}\text{) =}\text{5}\text{2}$ is assumed. This result, unlike the branching ratios calculated for the $\text{J(}{}^{11}{}_{\mathrm{\Lambda }}\text{B}\text{) =}\text{7}\text{2}$ case, is in accord with experiment and lends support to the assumption that $\text{J =}\text{5}\text{2}$ holds for ¹¹_ΛB. The necessity of the reinterpretation of some of the so-called ¹³_ΛC events in terms of ${}^{11}{}_{\mathrm{\Lambda }}\text{B}\text{→ π}{}^{\mathrm{?}}\text{+}{}^{11}\text{C}{}^1$ is indicated.     

3Σu−-3Σu+ coupling in the O2B3Σu− predissociation

The role of $\text{B}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}\text{-2}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$ spin-orbit mixing in the O₂ Schumann-Runge predissociation is investigated. The $\text{2}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$ state is found to cross the $\text{B}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}$ state near 2.0 Å with an interaction matrix element of approximately 55 cm^?1. This state contributes to the widths of the Bv ≥ 6 levels, but introduces only small level shift perturbations. When the partial widths due to the ${}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}\text{-}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$ interaction are added to the previously calculated widths due to the ⁵Π_u, ³Π_u, and ¹Π_u states, reasonable agreement is obtained with experimental measurements on O¹⁶O¹⁶ and O¹⁸O¹⁸. The possibility of non-Lorentzian line profiles and the dependence of the width on rotational quantum number is investigated. The approximation of the spin-orbit matrix element by its value at the crossing point is shown to be a good approximation for calculating the second difference perturbations.     

In-beam study of 144Gd

A level scheme of ¹⁴⁴Gd has been established using the ¹⁴⁴Sm(α, 4nγ) reaction and in-beam spectroscopy methods. Excitation functions, γ-ray angular distributions, γ-γ coincidence spectra, γ-spectra time related to the cyclotron beam bursts and conversion coefficients for the delayed transitions have been measured.The level scheme comprises 11 levels with spins up to I = 12. Two isomers, a 13 ± 2 ns, 7^? state at 2471.4 keV and a 145 ± 30 ns, 10⁺ state at 3433.0 keV have been observed. The former has similar excitation energy as the 7^? isomers in ¹⁴²Sm, ¹⁴⁰Nd and ¹³⁸Ce and it may arise from the $\text{{ν}\text{d}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}{}^{\mathrm{?1}}\text{× ν}\text{h}{}_{\mathrm{<mtext>11</mtext><mtext>2</mtext>}}{}^{\mathrm{?1}}\text{}}$ configuration although its lifetime seems to indicate some degree of collectivity. The 10⁺ state has a similar excitation energy as the 10⁺ isomer found in ¹³⁸Ce and it may arise from the dominant $\text{ν}\text{h}{}_{\mathrm{<mtext>11</mtext><mtext>2</mtext>}}{}^{\mathrm{?2}}$ configuration. Below the 10⁺ isomer in ¹⁴⁴Gd only two excited states have positive parity; the hitherto known first 2⁺ and 4⁺ states. The 11⁺ and 12⁺ states must include four-particle configurations or they have to be of collective nature. The latter possibility is supported by the considerable E2/M1 mixture (≈ 20 %) observed for the 11⁺ to 10⁺ transition. An analysis of the systematics of ground band levels in the N = 80 isotones shows the same gradual behavior between the two VMI solutions previously found for the Te isotopes.     

Lifetime of electronic states of CO2+

The radiative lifetimes of the $\text{A}\text{?}{}^2\text{Π}{}_{\mathrm{u}}$ and $\text{B}\text{?}{}^2\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$ states of CO₂⁺ were measured by means of the delayed coincidence method. Excitation was performed by a pulsed electron beam incident on CO₂. The results of these measurements are 115 ± 5 nsec for the $\text{A}\text{?}{}^2\text{Π}{}_{\mathrm{u}}$ state and 126 ± 3 nsec for the $\text{B}\text{?}{}^2\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$ state.     

Absolute E1, ΔK = 1 transition probabilities between multi-quasiparticle high-spin states in 176Hf and 178Hf

Applying the generalized centroid shift method in (α, 2n) reactions, the half-lives of the 3080 keV 15⁺ state in ¹⁷⁶Hf and of the 1637 keV 5^? state in ¹⁷⁸Hf have been measured as $\text{T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 0.20}{}^{\mathrm{+0.12}}{}_{\mathrm{?0.08}}\text{ns}$ and $\text{T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 0.40 ± 0.10}\text{ns}$, respectively. B(El) values of K-allowed E1 transitions $\text{n}\text{9}\text{2}{}^{\mathrm{+}}\text{[624]→}\text{7}\text{2}{}^{\mathrm{?}}\text{[514]}$ are derived, and together with other data on similar transitions in odd-A nuclei, compared with predictions of the Nilsson plus pairing model. In ¹⁷⁶Hf, the 15⁺ and 14^? states at 3080 and 2866 keV, respectively, appear as quite pure deformed 4QP configurations. In the 2QP state at 1637 keV in ¹⁷⁸Hf, possible strong mixing of vibrational components is discussed coupled via 2QP K-admixtures arising from the partial alignment of the $\text{i}{}_{\mathrm{<mtext>13</mtext><mtext>2</mtext>}}$ neutron.     

Predissociation and Λ-doubling in the even-parity Rydberg states of the nitrogen molecule

Predissociations in the y¹Π_g and $\text{x}{}^1\text{Σ}{}_{\mathrm{g}}{}^{\mathrm{?}}$ Rydberg states of N₂ (configurations $\text{1π}{}_{\mathrm{u}}{}^{\mathrm{?1}}\text{4pσ}$ and $\text{1π}{}_{\mathrm{u}}{}^{\mathrm{?1}}\text{3pπ}$, respectively) and their likely causes, are discussed. Peaking of rotational intensity at unusually low J values, without sharp breaking off, is interpreted as due to case c^? or case cⁱ predissociation. Λ doubling in the y state, attributed to interactions with the $\text{x}{}^1\text{Σ}{}_{\mathrm{g}}{}^{\mathrm{?}}$ state and with another, ¹Σ⁺, state of the same electron configuration as x, is analyzed. From this analysis the location of the (unobserved) ${}^1\text{Σ}{}_{\mathrm{g}}{}^{\mathrm{+}}$ state, here labeled x′, is obtained. It is concluded that the predissociation in the Π⁺ levels of the y state is an indirect one mediated by the interaction with x′ coupled with predissociation of x′ by a ${}^3\text{Σ}{}_{\mathrm{g}}{}^{\mathrm{?}}$ state dissociating to ${}^4\text{S +}{}^2\text{P}$ atoms: combined, however, with perturbation of the y state by the k¹Π_g Rydberg state (configuration $\text{3σ}{}_{\mathrm{g}}{}^{\mathrm{?1}}\text{4dπ}$), whose Π⁺ levels are completely predissociated.     

The emission spectra of H35Cl+, H37Cl+, D35Cl+, and D37Cl+ in the region 2700–4100 Å

The $\text{A}{}^2\text{Σ}{}^{\mathrm{+}}\text{-X}{}^2\text{Π}$ emission spectrum of HCl⁺ has been measured and analyzed for four isotopic combinations. These analyses extend previous work and provide rotational constants for the v = 0–2 levels of the ground state and for the v = 0–9 levels of the excited state. RKR potentials have been determined for both states, although the upper state could not be fitted precisely to such a model. Calculated relative intensities based on these potentials demonstrated that the electronic transition moment must change rapidly with lower state vibrational quantum number. Although considerable caution should be exercised in applying the concept of equilibrium constants to the $\text{A}{}^2\text{Σ}{}^{\mathrm{+}}$ state, the following are the best estimates of these constants (in cm^?1) for the $\text{X}{}^2\text{Π}$ state of H³⁵Cl⁺: B_e = 9.9406, ω_e = 2673.7, A_e = ? 643.7, and $\text{r}{}_{\mathrm{e}}\text{= 1.315}\text{A}\text{?}$. For the $\text{A}{}^2\text{Σ}{}^{\mathrm{+}}$ state of H³⁵Cl: T_e = 28 628.08, B_e ～ 7.505, ω_e ～ 1606.5, and $\text{r}{}_{\mathrm{e}}\text{= 1.514}\text{A}\text{?}$.     

Nuclear magnetic moment of the 9.7 h 12− isomer 196mAu

The magnetic hyperfine splitting v_M=|gμ_NB_HF/h| of ^196mAu (j^π=12^?; configuration ¦(π$\text{11}\text{2}$($\text{v}\text{13}\text{2}{}^{\mathrm{+}}\text{)〉}{}_{12}{}^{\mathrm{?}}$; $\text{T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 9.7}\text{h}\text{)}$ as dilute impurity in Ni has been determined with nuclear magnetic resonance on oriented nuclei as 96.0(2) MHz. With the known hyperfine field B_HF = ?264.4(3.9) kG corrected for hyperfine anomalies the g-factor and magnetic moment of ^196mAu are deduced to be |g| = 0.476(7) and |μ| = 5.72(8) μ_N. Taking into account the known magnetic properties of $\text{π}\text{1}\text{2}{}^{\mathrm{?}}$ and $\text{v}\text{13}\text{2}{}^{\mathrm{+}}$ isomeric states in the neighbouring odd Pt, Au and Hg nuclei the structure of the 12^? state is discussed.     

The rotational spectrum of the X 2Σ+ state of the SrF radical using laser microwave optical double resonance

The pure rotational spectrum of the $\text{X}{}^2\text{Σ}{}^{\mathrm{+}}$ state of the gaseous SrF radical has been measured using microwave optical double resonance (MODR) techniques. The analysis fully confirms the recent dye laser excitation spectrum and rotational assignment of the $\text{B}{}^2\text{Σ}{}^{\mathrm{+}}\text{-X}{}^2\text{Σ}{}^{\mathrm{+}}$ system. Transitions were measured in both the v″ = 0 and v″ = 1 states to give values of B_e″ = 0.250533 cm^?1, α_e″ = 1.546 × 10^?3 cm^?1 and γ″ (spin-rotation) = 2.49 × 10^?3 cm^?1. General qualitative features of MODR in ²Σ⁺ states are treated and suggested improvements for obtaining experimental hyperfine constants are discussed. The more precise ground state constants are merged with the B-X optical analysis to obtain a more accurate set of constants for both states.     

Resonance neutron capture gamma rays in 177Hf

Primary capture γ-rays have been studied for 38 ¹⁷⁷Hf neutron resonances with energies in the range 1–165 eV. Intensities were measured for 29 transitions ending at states with an excitation energy in ¹⁷⁸Hf up to 2050 keV. The analysis was facilitated by the previous knowledge of the spin and parity of all neutron resonances and of most low-lying states. For nine final levels, which had not previously been seen, information on J and π was deduced from the corresponding average intensities. The distribution of partial widths was fitted with a χ² function with ν = 1.38_?0.13^+0.18 degrees of freedom for E1 radiation and ν = 1.5_?0.40^+0.60 for M1 radiation. The average El reduced photon strength was found to be $\text{S}{}_{\mathrm{<mtext>El</mtext>}}\text{= 〈Γ}{}_{\mathrm{\gamma itij}}\text{/DE}{}_{\mathrm{\gamma }}{}^5\text{〉A}{}^{\mathrm{<mtext>?8</mtext><mtext>3</mtext>}}\text{= (4.8 ± 1.0) × 10}{}^{\mathrm{?15}}\text{MeV}{}^{\mathrm{?5}}$ and the ratio between El and Ml intensities equal to 5.5 ± 1.4. A comparison of this value for the El strength with those reported for other nuclei with A$\text{\$}\text{?}$= 100 showed that the intensities follow the A-dependence predicted by the Brink-Axel model. A non-statistical effect was observed, consisting of an enhancement of El transition probalilities to K = 2, 3 final states as compared to K = 0, 4 states.     

Analysis of the B′3Σu− → B3Πg (0,0) emission band of molecular nitrogen

The (0,0) band of the $\text{B′}\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}\text{→ B}{}^3\text{Π}{}_{\mathrm{g}}$ emission (Infrared Afterglow) system of molecular nitrogen has been recorded with a resolution of 0.046 cm^?1 and a line position accuracy of 0.007 cm^?1. Six hundred and seventy-two lines are tabulated into a line list for the 1.53 μm (low-resolution) emission feature. Of these, 482 are assigned as members of the 27 branches of the B′ → B transition, while 150 are identified with the 1PG (3,6) band. Molecular constants for the v = 0 levels of the $\text{B′}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}$ and B³Π_g states have been computed and tabulated.     

Structural connections between 148Sm and 149Sm nuclei

The ^{146, 148}Nd(α, χn) and ^{148, 150}Nd(³He, χn) reactions at E_α = 20–43 MeV and E_3He = 19–27 MeV, are used to study excited states in the ¹⁴⁹Sm₈₆ and ¹⁴⁹Sm₈₇ nucleides and consequently the low-spin odd-parity excitation. The mixing ratios and multipolarities of the most prominent transitions are deduced from the combined evidence of angular distribution and electron conversion data. The spin-parity assignments for most of the levels observed are established. In ¹⁴⁸Sm the ground state band extending to I^π = 10⁺ is predominantly populated. A negative-parity odd-spin band extending from I^π = 3^?through 11^? is also observed. The bands in ¹⁴⁸Sm are interpreted within the framework of the interacting boson approximation model. In ¹⁴⁹Sm positive-parity levels with spin up to $\text{25}\text{2}$ and negative-parity levels with spins up to $\text{21}\text{2}$ are observed. The predominant γ-decay proceeds via transitions associated with $\text{i}{}_{\mathrm{<mtext>13</mtext><mtext>2</mtext>}}$, $\text{h}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}$, $\text{f}{}_{\mathrm{<mtext>7</mtext><mtext>2</mtext>}}$ and $\text{h}{}_{\mathrm{<mtext>11</mtext><mtext>2</mtext>}}$ intrinsic configurations. The branching ratios B(E1)/B(E2) are calculated and compared in both ¹⁴⁸Sm and ¹⁴⁹Sm nucleides. The B(E1)/B(E2) dependence on the value of Z for some N = 86 (as well as 88 and 84) isotones showing a minimum of Z = 64 was noted. A 4 ns high-spin isomer mainly decaying into the positive-parity band based on the $\text{i}{}_{\mathrm{<mtext>13</mtext><mtext>2</mtext>}}$ state in ¹⁴⁹Sm is found. Experimental evidence is presented to interprete the $\text{1}\text{2}{}^{\mathrm{+}}$, $\text{15}\text{2}{}^{\mathrm{+}}$, … and $\text{9}\text{2}{}^{\mathrm{?}}$, $\text{13}\text{2}{}^{\mathrm{?}}$, …, ΔI = 2, sequences in ¹⁴⁹Sm as arising from the coupling of an $\text{h}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}$ neutron to the octupole and quadrupole modes of the ¹⁴⁸Sm core nucleus. The absolute reaction cross sections for the ^{146, 148, 150}Nd(³He, χn) reactions have been determined for different bombarding energies. The mixing of the $\text{f}{}_{\mathrm{<mtext>7</mtext><mtext>2</mtext>}}$ and $\text{h}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}$ shells is discussed in the framework of an axial-particle-rotor model calculation.     

Polarization spectroscopy of the E0g+-B0u+ band system of Br2

The E-B (0_g⁺-0_u⁺) band system of Br₂ has been investigated at Doppler-limited resolution using polarization labeling spectroscopy. Merged E state data for the three naturally occurring isotopes in the range v_E = 0–16, expressed in terms of the constants for ⁷⁹Br₂, are (in cm^?1) Y_0,0 = 49 777.962(54), Y_1,0 = 150.834(22), Y_2,0 = ?0.4182(28), Y_3,0 = 6.6(11) × 10^?4, Y_0,1 = 4.1876(28) × 10^?2, Y_1,1 = ?1.607(16) × 10^?4, and Y_0,2 = 1.39(39) × 10^?8. The bond distance is $\text{r}{}_{\mathrm{<mtext>e</mtext>}}\text{= 3.194}\text{A}\text{?}$, and the diabatic dissociation energy to $\text{Br}{}^{\mathrm{+}}\text{(}{}^3\text{P}{}_2\text{) +}\text{Br}{}^{\mathrm{?}}\text{(}{}^1\text{S}{}_0\text{)}\text{is 34 700 cm}{}^{\mathrm{?1}}$.     

The spectrum of HeNe+

Discharges through mixtures of helium and neon show two band groups near 4250 and 4100 Å as first observed by Druyvesteyn. These bands, assigned to the HeNe⁺ ion by Tanaka, Yoshino, and Freeman, have been studied under high resolution and have been fairly completely analyzed. The upper state of the transition is a very weakly bound state resulting from $\text{He}{}^{\mathrm{+}}\text{(}{}^2\text{S) +}\text{Ne}\text{(}{}^1\text{S}{}_0\text{)}$. There are two lower states resulting from the two components of $\text{Ne}{}^{\mathrm{+}}\text{(}{}^2\text{P) +}\text{He}\text{(}{}^1\text{S}{}_0\text{)}$. The upper of these two (${}^2\text{Π}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$) is also very weakly bound while the lower of the two, the ²Σ⁺ ground state, has a dissociation energy of 0.69 eV and an r_e value of 1.30 Å. All bands in both band groups show four branches designated R_ff, Q_ef, Q_fe, and P_ee. From their analysis the rotational constants in the various vibrational levels of the three electronic states have been determined. While no spin splitting in the B²Σ⁺ state has been found the ground state X²Σ shows a very large spin splitting and the $\text{A}{}_2{}^2\text{Π}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$ state a very large $\text{Ω-type}$ doubling. The vibrational numberings in all these states were established by the study of the spectrum of ³HeNe⁺. At the same time the hyperfine structure observed in all lines of ³HeNe⁺ confirmed the nature of the upper state B²Σ⁺ as resulting from He⁺ + Ne, i.e., by charge exchange from the ground state. The ${}^2\text{Π}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$ component of the ²Π state has not been observed, presumably because of low intensity.     

The 85Rb(p,d)84Rb reaction

The spectrum seen in single neutron pickup leading to the doubly odd nucleus ⁸⁴Rb is remarkably clean, with only five levels populated by l = 4 and six by l = 1 transitions. A simple 2J+1 weighting for the l = 4 data, combined with previous information on ⁸⁴Rb, allowed the J^π = 2^?–7^? states of the ($\text{v}\text{g}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}{}^{\mathrm{?3}}\text{? π}\text{f}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}{}^{\mathrm{?3}}$) multiplet to be identified. These data are used to determine the two-hole $\text{π}\text{f}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}{}^{\mathrm{?1}}\text{-v}\text{g}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}{}^{\mathrm{?}}$ interaction matrix elements.     

Molecular Rydberg transitions: Cyanogen chloride

The electronic absorption spectrum of cyanogen chloride has been investigated in the range 2200-1250 Å. The first s-Rydberg transitions, $\text{X}\text{?}{}^1\text{Σ}{}^{\mathrm{+}}\text{→}{}^3\text{Π}{}_1$ and $\text{X}\text{?}{}^1\text{Σ}{}^{\mathrm{+}}\text{→}{}^1\text{Π}{}_1$ have been assigned, and analyzed to yield exchange and spin-orbit coupling parameters. The relative intensities of these two transitions have been shown to accord with an intermediate coupling situation. The $\text{π → π}{}^1$ intravalence excitations, leading to ^1.3(Σ^?, Δ and Σ⁺) states, have been discussed. It has been shown that one or both of the ¹Σ^? and ¹Δ states have bent geometries and that the ¹Σ⁺ state is located (tentatively) at 79 755 cm^?1. Two $\text{σ → π}{}^1\text{π → σ}{}^1$ states have been assigned, one at 56 340 cm^?1, the other at 74 450 cm^?1. The latter assignment is tentative, being largely based on observed vibronic interferences between the $\text{X}\text{?}{}^1\text{Σ}{}^{\mathrm{+}}\text{→}{}^1\text{Π}{}_1$ transition and the 74 450 cm^?1 transition. A considerable amount of vibrational oscillator strength and quantum defect data is presented.