- About this Journal ·
- Abstracting and Indexing ·
- Advance Access ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
The Scientific World Journal
Volume 2013 (2013), Article ID 652124, 7 pages
Solvation Effects on the Static and Dynamic First-Order Electronic and Vibrational Hyperpolarizabilities of Uracil: A Polarized Continuum Model Investigation
Department of Chemistry, University of Catania, Viale A. Doria 6, Catania 95125, Italy
Received 27 August 2013; Accepted 18 September 2013
Academic Editors: T. S. Chu, T. Ebata, P. Orea, and R. Schweiss
Copyright © 2013 Andrea Alparone. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Electronic () and vibrational () first-order hyperpolarizabilities of uracil were determined in gas and water solution using the Coulomb-attenuating Density Functional Theory level with the Dunning’s correlation-consistent aug-cc-pVDZ basis set. Frequency-dependent values were computed for the Second Harmonic Generation (SHG) and Electric Optical Pockels Effect (EOPE) nonlinear optical phenomena. The Polarized Continuum Model was employed to study the solvent effects on the electronic and vibrational properties. The introduction of solvation contributions increases the (static) value by ca. 110%. In comparison, smaller enhancements are found for the (EOPE) and (SHG) data evaluated at the typical wavelength of 694 nm (by 40–50%). The gas-water hyperpolarizability difference was rationalised through a density analysis study. The magnitudes of the vibrational first-order hyperpolarizabilities are comparable to their electronic counterparts and noticeably increase in solution: (EOPE) ~ (EOPE) in aqueous phase at nm. Analysis of the IR and Raman spectra is useful to elucidate the most important contributing modes to the vibrational first-order hyperpolarizabilities.
Organic nonlinear optical (NLO) compounds are intensively studied, primarily for their potential use in the design of photonic and optoelectronic devices [1–3]. Biomolecules are attractive NLO materials, having the practical advantage to be already available in nature. Over recent years, DNA-based systems have received great attention for their conductive and NLO applications [4–12]. Nevertheless, characterization of the NLO properties of single nucleic acid bases is still rather incomplete. To the best of our knowledge, experimental response electric properties of the smallest base uracil are not available so far, whereas some theoretical estimates of the electronic polarizabilities () [13–21] and second-order hyperpolarizabilities ()  were previously reported. However, there is significant interest in exploring the second-order NLO effects, which are important for immediate practical applications. At the microscopic level, the second-order NLO properties are associated with the first-order hyperpolarizability tensor (), which originates from the responses of a molecular system to external electric field strengths Fi, producing an induced dipole moment ():
Recently, pure vibrational contributions to the first-order hyperpolarizability of uracil have been calculated in vacuum through a Lanczos procedure , whereas explorations of solvent effects on the electronic and vibrational values are still lacking to date.
Our current computational study mainly focuses on the electronic () and vibrational () static and dynamic first-order hyperpolarizabilities of uracil. The fundamental role of the vibrational counterparts to the hyperpolarizabilities has been widely documented . The present calculations were performed in gas and water solution under the Polarized Continuum Model (PCM) approximation [24, 25]. There are many indications in the literature showing that calculated first-order hyperpolarizabilities of organic molecules are strongly affected by solvent contributions [26–33]. Solvation effects on the electronic and vibrational [18, 19] and  values of uracil have been previously explored by means of PCM Hartree-Fock and DFT computations in carbon tetrachloride, acetonitrile, and water solutions.
2. Computational Methods
The present calculations were performed in the gas phase and water solution with the Gaussian 09 package . The solvent effects were entirely modelled under the PCM approximation as implemented in the Gaussian 09 program. The geometry of uracil was optimized under the planar symmetry using the CAM-B3LYP functional  and the polarised and diffuse Dunning’s correlation-consistent aug-cc-pVDZ basis set . The IR and Raman spectra were simulated under the harmonic approximation at the CAM-B3LYP/aug-cc-pVDZ level on the geometries optimized at the same level. The structures are true minima on the potential energy surfaces (no imaginary wavenumbers).
Static values were calculated at the CAM-B3LYP/aug-cc-pVDZ//CAM-B3LYP/aug-cc-pVDZ level. We selected the CAM-B3LYP functional and aug-cc-pVDZ basis set considering their satisfactory performances in the prediction of the response electric properties of organic compounds, reproducing adequately first-order hyperpolarizabilities obtained using high-level correlated ab initio methods and larger basis sets [28, 29, 37–45]. The dynamic electronic first-order hyperpolarizabilities for the Second Harmonic Generation [SHG, ] and Electric Optical Pockels Effect [EOPE, ] NLO phenomena were calculated at the CAM-B3LYP/aug-cc-pVDZ level in the range 0–0.06563 a.u. The highest value corresponds to the wavelength () of 694 nm, which is characteristic of the ruby laser.
Static pure vibrational first-order hyperpolarizabilities were obtained at the CAM-B3LYP/aug-cc-pVDZ//CAM-B3LYP/aug-cc-pVDZ level in vacuum and water solution under the double-harmonic approximation (the used symbols have their standard meaning) :
By assuming the validity of the infinity frequency approximation , the (SHG) and (EOPE) processes are, respectively,
In this study we report the invariant first-order hyperpolarizabilities () : where () is given by .
Atomic units are used throughout the work. Conversion factor to the SI is: 1 a.u. of .
3. Results and Discussion
Table 1 lists the CAM-B3LYP/aug-cc-pVDZ dipole moments. The largest component lies along the z-axis, recovering ca. 96% of the total value. The gas phase (CAM-B3LYP/aug-cc-pVDZ) of 4.57 D overestimates by 18% the experimental datum obtained by microwave measurements [(exp.) 3.87 D] , being in good agreement with the high-level ab initio CCSD(T)/aug-cc-pVDZ estimate of 4.33 D (+5.5%) . The introduction of the solvation contributions increases the value by 1.4 D (+37%), in qualitative consistency with the observed increase of 0.26 D when passing from the gas phase  to dioxane solution .
Table 1 also includes the static electronic first-order hyperpolarizability tensor components (; ) in gaseous and aqueous phases. In gas, is in absolute value the predominant component (−106.5 a.u.), whereas in water solution the largest components are a.u.) and (262.3 a.u.). When passing from the gas phase to the water solution, the value increases by about a factor of two, whereas on the contrary decreases by ca. a factor of two. From the present computations, dominates the first-order hyperpolarizability of both the gaseous and aqueous phases, giving ca. 85% and 99% of the value, respectively.
In order to clarify the solvation effects on the response electric properties, we determined the spatial contributions of electrons to the first-order hyperpolarizabilities by computing density of hyperpolarizability amplitudes, [50, 51]. The is defined as derivative of the charge density function with respect to applied electric field strengths ( is the position vector). The is usually expanded in powers of : For a certain positive-negative pair, the sign is positive when the direction of the positive to negative density is coincident with the positive direction of the chosen coordinate system (Figure 1), whereas the magnitude is proportional to the distance between the two densities. Following the current calculations, the main contribution to is given by the component, recovering ca. () and () of the () values in gas and water solution, respectively. Therefore, we explored the densities at the CAM-B3LYP/aug-cc-pVDZ level using the numerical procedure previously illustrated by Yamada and coworkers . The results evaluated at the isosurface of 0.25 a.u. are illustrated in Figure 2. As can be appreciated from the graphical representations, the distribution in the water solution is almost similar to that predicted in vacuum even if the amplitudes are much more spread out. This result is in some consistency with the calculated static values, with the (water)/(gas) and (water)/(gas) ratios being computed to be 2.3 and 2.1, respectively. Note that the above ratios are somewhat greater than those previously predicted for the average (1.3) and (1.5) properties by HF/aug-cc-pVDZ computations .
Figure 3 displays the frequency-dependent first-order hyperpolarizabilities computed in gaseous and aqueous phases in the 0–0.06563 range for the SHG and EOPE NLO processes. It is important to notice that resonance enhancement effects for the SHG phenomenon are expected to be rather marginal, since the experimental lowest-energy absorption being placed at 5.08 eV (0.1867 a.u.) in vapour  and 4.77 eV (0.1753 a.u.) in water solution  is sufficiently far from the highest 2 value of 0.1307 a.u. Not surprisingly, in the gas phase . The dispersion effects evaluated at the a.u. increase the static values by 13.7% for the EOPE and by for the SHG process. On the other hand, in aqueous phase the dispersion effects are significantly reduced, mainly due to incomplete responses of polar solvents as modelled by the PCM treatment [31–33, 54]. As can be appreciated from Figure 3, in water solution for the values between 0.01 and 0.04 a.u., whereas at 0.045 a.u. It is worth noting that at the value of 0.06563 a.u. the dispersion effect is negative for the EOPE phenomenon, with the (water) value being decreased by ca. 16.0% with respect to the static datum. On the other hand, in the case of the SHG process in water solution, the dispersion effect at a.u. is still positive as for the gas phase, even if it is noticeably inferior (+15.5%). As a consequence, although the static and dynamic electronic first-order hyperpolarizabilities in water solution are greater than the corresponding data in gas (compare the curves in Figure 3), the dispersion effects reduce the (water)/(gas) ratios, which are predicted to be 2.1, 1.53 and 1.48, respectively, for the static, EOPE, and SHG processes at a.u.
Beside the electronic first-order hyperpolarizability, we explored the solvation effects on the pure vibrational counterpart for the EOPE phenomenon. In a recent theoretical study, Christiansen and coworkers have determined the pure vibrational first-order hyperpolarizabilities of uracil in gas using VCI computations and the Lanczos algorithm . However, their reported data refer to the static and SHG process and are not directly comparable to our results. Figure 4 shows the CAM-B3LYP/aug-cc-pVDZ data in gaseous and aqueous phases over the 0–4000 cm−1 wavenumbers range. The largest contributions originate from the spectral region between 1500 and 2000 cm−1. Table 2 summarizes the main vibrational contributions to the values, also including the vibrational wavenumbers, IR intensities (), and Raman activities (ARaman). The highest-energy region (wavenumbers cm−1), entirely characterized by C–H and N–H stretching vibrations, furnishes only modest contributions to the data, principally owing to the high-wavenumber values. On the other hand, the low-energy modes (wavenumbers cm−1) produce small and moderate contributions, since the vibrational transitions are rather weak in the IR [IIR()2] and Raman [ARaman ()2] spectra. As for the pure vibrational polarizabilities , in both the gas phase and water solution, the largest values originate from the C=O stretching vibrations with the nonnegligible contribution of the in-plane N-H bending deformation (modes and ). A graphical representation of the atomic displacement vectors involved in these vibrational modes is displayed in Figure 5. These transitions located at 1802 cm−1 () and 1828 cm−1 () by the present calculations in vacuum exhibit the strongest absorption peaks in the IR spectrum (Figure 6), with the IIR values of 902 and 607 km/mol, respectively. Note that the and modes are also active in the Raman spectra (ARaman 58 and 29 amu, resp.). As a result, the values originated by the and transitions contribute, respectively, to ca. 89% and 50% of the total datum. In water solution (Figure 6), the wavenumbers of the and vibrations are downward shifted, respectively, by ca. 80 cm−1 (−4.5%) and 60 cm−1 (−3.2%) with respect to the gas phase, with the IIR values being concomitantly increased by ca. 131% and 45%, respectively. In addition, when passing from the gaseous to the aqueous phase, the ARaman() and ARaman() values enhance by ca. a factor of two and four, respectively. Therefore as for the values, the solvent contributions are expected to play a crucial role also for the vibrational first-order hyperpolarizabilities of uracil, increasing the values of the and modes by 69.4 a.u. (+120%) and 38.5 a.u. (+119%). As can be appreciated by the data reported in Table 2, for both the phases other relevant contributions are given by the ring stretching modes as well as by the in-plane ring bending deformations, owing to their relatively low wavenumbers and moderate IIR and ARaman values. On the whole, the introduction of solvent contributions increases the total by ca. 130 a.u., with the (water)/(gas) ratio being predicted to be ca. three. Finally, it is worth noting that, at 0.06563 a.u. on going from the gas phase to water solution, the ratio is almost doubled, increasing from 0.46 to 0.91.
We have examined the effects of solvation on the static and frequency-dependent electronic and vibrational first-order hyperpolarizabilities of uracil. The properties were modeled in vacuum as well as in water solution using the PCM approach. The calculations were carried out using the long-range corrected CAM-B3LYP functional with the Dunning’s correlation-consistent aug-cc-pVDZ basis set. The introduction of solvent contributions significantly increases both the electronic and vibrational first-order hyperpolarizabilities. However, the dispersion effects on the electronic hyperpolarizabilities for the EOPE and SHG NLO phenomena are noticeably reduced when passing from the gas phase to the water solution. The magnitudes of the vibrational properties are comparable to the electronic counterparts, with the ratio increasing with the solvation and (water)(water) for the EOPE process at the characteristic wavelength of 694 nm. The most relevant contributing modes to the values principally involve the very intense infrared C=O stretching + N-H in-plane bending deformation vibrations.
Conflict of Interests
The author declares that there is no conflict of interests regarding the publication of this paper.
- D. S. Chemla and J. Zyss, Eds., Nonlinear Optical Properties of Organic Molecules and Crystals, vol. 1-2, Academic Press, San Diego, Calif, USA, 1987.
- P. N. Prasad and D. J. Williams, Introduction to Nonlinear Optical Effects in Molecules and Polymers, John Wiley & Sons, New York, NY, USA, 1991.
- H. S. Nalwa and S. Miyata, Eds., Nonlinear Optics of Organic Molecules and Polymers, CRC Press, Boca Raton, Fla, USA, 1997.
- L. Wang, J. Yoshida, N. Ogata, S. Sasaki, and T. Kajiyama, “Self-assembled supramolecular films derived from marine deoxyribonucleic acid (DNA)-cationic surfactant complexes: large-scale preparation and optical and thermal properties,” Chemistry of Materials, vol. 13, no. 4, pp. 1273–1281, 2001.
- H. Yan, X. Zhang, Z. Shen, and N. C. Seeman, “A robust DNA mechanical device controlled by hybridization topology,” Nature, vol. 415, no. 6867, pp. 62–65, 2002.
- D. Porath, G. Cuniberti, and R. D. Felice, “Charge transport in DNA based devices,” in Long Range Charge Transfer in DNA II. Topics in Current Chemistry, G. B. Schuster, Ed., vol. 237, pp. 183–227, Springer, Heidelberg, Germany, 2004.
- R. G. Endres, D. L. Cox, and R. R. P. Singh, “Colloquium: the quest for high-conductance DNA,” Reviews of Modern Physics, vol. 76, no. 1, pp. 195–214, 2004.
- J. G. Grote, J. A. Hagen, J. S. Zetts et al., “Investigation of polymers and marine-derived DNA in optoelectronics,” Journal of Physical Chemistry B, vol. 108, no. 25, pp. 8584–8591, 2004.
- H. Cohen, C. Nogues, R. Naaman, and D. Porath, “Direct measurement of electrical transport through single DNA molecules of complex sequence,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 33, pp. 11589–11593, 2005.
- C. F. Guerra, T. Van Der Wijst, and F. M. Bickelhaupt, “Nanoswitches based on DNA base pairs: why adenin-thymine is less suitable than guanine-cytosine,” ChemPhysChem, vol. 7, no. 9, pp. 1971–1979, 2006.
- A. J. Steckl, “DNA-a new material for photonics?” Nature Photonics, vol. 1, no. 1, pp. 3–5, 2007.
- H. Cohen, T. Sapir, N. Borovok et al., “Polarizability of G4-DNA observed by electrostatic force microscopy measurements,” Nano Letters, vol. 7, no. 4, pp. 981–986, 2007.
- C. T. Campos and F. E. Jorge, “Basis set convergence of electric properties in HF and DFT calculations of nucleic acid bases,” International Journal of Quantum Chemistry, vol. 109, no. 2, pp. 285–293, 2009.
- N. P. Labello, A. M. Ferreira, and H. A. Tcurtz, “An augmented effective core potential basis set for the calculation of molecular polarizabilities,” Journal of Computational Chemistry, vol. 26, no. 14, pp. 1464–1471, 2005.
- P. G. Jasien and G. Fitzgerald, “Molecular dipole moments and polarizabilities from local density functional calculations: application to DNA base pairs,” The Journal of Chemical Physics, vol. 93, no. 4, pp. 2554–2560, 1990.
- R. C. Johnson, T. D. Power, J. S. Holt et al., “Electron-correlated calculations of electric properties of nucleic acid bases,” Journal of Physical Chemistry, vol. 100, no. 48, pp. 18875–18881, 1996.
- H. Basch, D. R. Garmer, P. G. Jasien, M. Krauss, and W. J. Stevens, “Electrical properties of nucleic acid bases,” Chemical Physics Letters, vol. 163, no. 6, pp. 514–522, 1989.
- A. Alparone, “Linear and nonlinear optical properties of nucleic acid bases,” Chemical Physics, vol. 410, pp. 90–98, 2013.
- S. Millefiori and A. Alparone, “Tautomerism and polarizability in uracil: coupled cluster and density-functional theory study,” Chemical Physics, vol. 303, no. 1-2, pp. 27–36, 2004.
- T. Pluta, M. Kolaski, M. Medved’, and S. Budzák, “Dipole moment and polarizability of the low-lying excited states of uracil,” Chemical Physics Letters, vol. 546, pp. 24–29, 2012.
- T. P. Haley, E. R. Graybill, and S. M. Cybulski, “Ab initio calculations of dispersion coefficients for nucleic acid base pairs,” Journal of Chemical Physics, vol. 124, no. 20, Article ID 204301, 2006.
- M. B. Hansen, P. Seidler, W. Gyrffy, and O. Christiansen, “A Lanczos-chain driven approach for calculating damped vibrational configuration interaction response functions,” Journal of Chemical Physics, vol. 133, no. 11, Article ID 114102, 2010.
- D. M. Bishop, “Molecular vibration and nonlinear optics,” Advances in Chemical Physics, vol. 104, pp. 1–40, 1998.
- J. Tomasi, B. Mennucci, and R. Cammi, “Quantum mechanical continuum solvation models,” Chemical Reviews, vol. 105, no. 8, pp. 2999–3094, 2005.
- G. Scalmani and M. J. Frisch, “Continuous surface charge polarizable continuum models of solvation. I. General formalism,” Journal of Chemical Physics, vol. 132, no. 11, Article ID 114110, 2010.
- W. Bartkowiak and T. Misiaszek, “Solvent effect on static vibrational and electronic contribution of first-order hyperpolarizability of π-conjugated push-pull molecules: quantum-chemical calculations,” Chemical Physics, vol. 261, no. 3, pp. 353–357, 2000.
- R. Cammi, B. Mennucci, and J. Tomasi, “Solvent effects on linear and nonlinear optical properties of donor- acceptor polyenes: investigation of electronic and vibrational components in terms of structure and charge distribution changes,” Journal of the American Chemical Society, vol. 120, no. 34, pp. 8834–8847, 1998.
- A. Alparone, “Theoretical study of the electronic (hyper)polarizabilities of amino acids in gaseous and aqueous phases,” Computational and Theoretical Chemistry, vol. 976, pp. 188–190, 2011.
- A. Alparone, “Corrigendum to “Theoretical study of the electronic (hyper)polarizabilities of amino acids in gaseous and aqueous phases” [Comput. Theor. Chem. 976 (2011) 188–190],” Computational and Theoretical Chemistry, vol. 980, p. 144, 2012.
- A. Alparone and S. Millefiori, “Gas and solution phase electronic and vibrational (hyper)polarizabilities in the series formaldehyde, formamide and urea: CCSD(T) and DFT theoretical study,” Chemical Physics Letters, vol. 416, no. 4–6, pp. 282–288, 2005.
- R. Cammi, M. Cossi, B. Mennucci, and J. Tomasi, “Analytical Hartree-Fock calculation of the dynamical polarizabilities α, β, and γ of molecules in solution,” Journal of Chemical Physics, vol. 105, no. 23, pp. 10556–10564, 1996.
- R. Cammi, M. Cossi, B. Mennucci, and J. Tomasi, “Solvent effects on static and dynamic polarizability and hyperpolarizabilities of acetonitrile,” Journal of Molecular Structure, vol. 436-437, pp. 567–575, 1997.
- B. Mennucci, R. Cammi, M. Cossi, and J. Tomasi, “Solvent and vibrational effects on molecular electric properties. Static and dynamic polarizability and hyperpolarizabilities of urea in water,” Journal of Molecular Structure, vol. 426, no. 1–3, pp. 191–198, 1998.
- M. J. Frisch, G. W. Trucks, H. B. Schlegel et al., GAUSSIAN 09, Revision A.02, Gaussian, Wallingford, Conn, USA, 2009.
- T. Yanai, D. P. Tew, and N. C. Handy, “A new hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP),” Chemical Physics Letters, vol. 393, no. 1–3, pp. 51–57, 2004.
- D. E. Woon and T. H. Dunning, “Gaussian basis sets for use in correlated molecular calculations. IV. Calculation of static electrical response properties,” The Journal of Chemical Physics, vol. 100, no. 4, pp. 2975–2988, 1994.
- A. Alparone, “Electron correlation effects and density analysis of the first-order hyperpolarizability of neutral guanine tautomers,” Journal of Molecular Modeling, vol. 19, pp. 3095–3102, 2013.
- A. Alparone, “The effect of secondary structures on the NLO properties of single chain oligopeptides: a comparison between β-strand and α-helix polyglycines,” Physical Chemistry Chemical Physics, vol. 15, pp. 12958–12962, 2013.
- M. Medved, S. Budzák, and T. Pluta, “Static NLO responses of fluorinated polyacetylene chains evaluated with long-range corrected density functionals,” Chemical Physics Letters, vol. 515, no. 1–3, pp. 78–84, 2011.
- D. Jacquemin, E. A. Perpète, M. Medved et al., “First hyperpolarizability of polymethineimine with long-range corrected functionals,” Journal of Chemical Physics, vol. 126, no. 19, Article ID 191108, 2007.
- J. Urdaneta, Y. Bermúdez, F. Arrieta et al., “Theoretical study in gas phase of linear and nonlinear optical properties of the ortho-, meta- and para-nitrophenol isomers,” Theoretical Chemistry Accounts, vol. 126, no. 1, pp. 27–37, 2010.
- A. Alparone, “Comparative study of CCSD(T) and DFT methods: electronic (hyper)polarizabilities of glycine,” Chemical Physics Letters, vol. 514, no. 1–3, pp. 21–25, 2011.
- C.-C. Zhang, H.-L. Xu, Y.-Y. Hu, S.-L. Sun, and Z.-M. Su, “Quantum chemical research on structures, linear and nonlinear optical properties of the Li@n-acenes salt (, 2, 3, and 4),” Journal of Physical Chemistry A, vol. 115, no. 10, pp. 2035–2040, 2011.
- P. Krawczyk, “DFT study of linear and nonlinear optical properties of donor-acceptor substituted stilbenes, azobenzenes and benzilideneanilines,” Journal of Molecular Modeling, vol. 16, no. 4, pp. 659–668, 2010.
- S. Millefiori and A. Alparone, “Theoretical determination of the vibrational and electronic (hyper)polarizabilities of C4H4X (, S, Se, Te) heterocycles,” Physical Chemistry Chemical Physics, vol. 2, no. 11, pp. 2495–2501, 2000.
- D. M. Bishop, M. Hasan, and B. Kirtman, “A simple method for determining approximate static and dynamic vibrational hyperpolarizabilities,” The Journal of Chemical Physics, vol. 103, no. 10, pp. 4157–4159, 1995.
- V. Keshari, W. M. K. P. Wijekoon, P. N. Prasad, and S. P. Karna, “Hyperpolarizabilities of organic molecules: Ab initio time-dependent coupled perturbed Hartree-Fock-Roothaan studies of basic heterocyclic structures,” Journal of Physical Chemistry, vol. 99, no. 22, pp. 9045–9050, 1995.
- R. D. Brown, P. D. Godfrey, D. McNaughton, and A. P. Pierlot, “Microwave spectrum of uracil,” Journal of the American Chemical Society, vol. 110, no. 7, pp. 2329–2330, 1988.
- I. Kulakowska, M. Geller, and B. Lesyng, “Barrier to rotation and conformation of the NR2 group in cytosine and its derivatives. Part II. Experimental and theoretical dipole moments of methylated cytosines,” Biochimica et Biophysica Acta, vol. 407, no. 4, pp. 420–429, 1975.
- M. Nakano, I. Shigemoto, S. Yamada, and K. Yamaguchi, “Size-consistent approach and density analysis of hyperpolarizability: second hyperpolarizabilities of polymeric systems with and without defects,” The Journal of Chemical Physics, vol. 103, no. 10, pp. 4175–4191, 1995.
- S. Yamada, M. Nakano, I. Shigemoto, S. Kiribayashi, and K. Yamaguchi, “Intense electron correlation dependence of the first hyperpolarizabilities β of a nitroxide radical and formaldehyde,” Chemical Physics Letters, vol. 267, no. 5-6, pp. 445–451, 1997.
- L. B. Clark, G. G. Peschel, and I. Tinoco Jr., “Vapor spectra and heats of vaporization of some purine and pyrimidine bases,” Journal of Physical Chemistry, vol. 69, no. 10, pp. 3615–3618, 1965.
- D. Voet, W. B. Gratzer, R. A. Cox, and P. Doty, “Absorption spectra of nucleotides, polynucleotides, and nucleic acids in the far ultraviolet,” Biopolymers, vol. 1, no. 3, pp. 193–208, 1963.
- R. Cammi, L. Frediani, B. Mennucci, and K. Ruud, “Multiconfigurational self-consistent field linear response for the polarizable continuum model: theory and application to ground and excited-state polarizabilities of para-nitroaniline in solution,” Journal of Chemical Physics, vol. 119, no. 12, pp. 5818–5827, 2003.