Abstract
IR and polarized Raman spectra of CH3NH3NaSeO4 · 6H2O (MASS), NaNH4SeO4 · 2H2O (SAS), and their deuterated analogues are recorded and analyzed. In both the crystal symmetry of SeO2- 4 is lower than Td. The symmetry of CH3NH+ 3 is lower than C3v and hydrogen bonding is strong in MASS. NH+ 4 is not rotating freely in the crystal lattice of SAS. SERS spectra are recorded in two types of silver colloids. Colloid 1 adsorbs MASS through the nitrogen atom of CH3NH3 group. There are two different adsorption sites for MASS in colloid 2. SAS is chemisorbed by colloid 2 through the oxygen atom of SeO2- 4. Shifting and splitting observed for the internal modes of SeO2- 4 on adsorption are due to the reduced local symmetry of the ion.
| Original language | English |
|---|---|
| Pages (from-to) | 92-99 |
| Number of pages | 8 |
| Journal | Journal of Solid State Chemistry |
| Volume | 110 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 1994 May |
| Externally published | Yes |
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ASJC Scopus subject areas
- Materials Chemistry
- Physical and Theoretical Chemistry
- Inorganic Chemistry
Cite this
Infrared, Single Crystal Raman, and SERS Spectra of CH3NH3NaSeO4 · 6X2O and NaNH4SeO4 · 2X2O (X = H,D). / Philip, Daizy; Aruldhas, G.; Osaka, Tetsuya; Miyazaki, A.
In: Journal of Solid State Chemistry, Vol. 110, No. 1, 05.1994, p. 92-99.Research output: Contribution to journal › Article
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TY - JOUR
T1 - Infrared, Single Crystal Raman, and SERS Spectra of CH3NH3NaSeO4 · 6X2O and NaNH4SeO4 · 2X2O (X = H,D)
AU - Philip, Daizy
AU - Aruldhas, G.
AU - Osaka, Tetsuya
AU - Miyazaki, A.
PY - 1994/5
Y1 - 1994/5
N2 - IR and polarized Raman spectra of CH3NH3NaSeO4 · 6H2O (MASS), NaNH4SeO4 · 2H2O (SAS), and their deuterated analogues are recorded and analyzed. In both the crystal symmetry of SeO2- 4 is lower than Td. The symmetry of CH3NH+ 3 is lower than C3v and hydrogen bonding is strong in MASS. NH+ 4 is not rotating freely in the crystal lattice of SAS. SERS spectra are recorded in two types of silver colloids. Colloid 1 adsorbs MASS through the nitrogen atom of CH3NH3 group. There are two different adsorption sites for MASS in colloid 2. SAS is chemisorbed by colloid 2 through the oxygen atom of SeO2- 4. Shifting and splitting observed for the internal modes of SeO2- 4 on adsorption are due to the reduced local symmetry of the ion.
AB - IR and polarized Raman spectra of CH3NH3NaSeO4 · 6H2O (MASS), NaNH4SeO4 · 2H2O (SAS), and their deuterated analogues are recorded and analyzed. In both the crystal symmetry of SeO2- 4 is lower than Td. The symmetry of CH3NH+ 3 is lower than C3v and hydrogen bonding is strong in MASS. NH+ 4 is not rotating freely in the crystal lattice of SAS. SERS spectra are recorded in two types of silver colloids. Colloid 1 adsorbs MASS through the nitrogen atom of CH3NH3 group. There are two different adsorption sites for MASS in colloid 2. SAS is chemisorbed by colloid 2 through the oxygen atom of SeO2- 4. Shifting and splitting observed for the internal modes of SeO2- 4 on adsorption are due to the reduced local symmetry of the ion.
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U2 - 10.1006/jssc.1994.1140
DO - 10.1006/jssc.1994.1140
M3 - Article
AN - SCOPUS:0011176643
VL - 110
SP - 92
EP - 99
JO - Journal of Solid State Chemistry
JF - Journal of Solid State Chemistry
SN - 0022-4596
IS - 1
ER -