Compound and photoelectric device, image sensor, and electronic device including the same

1. A compound represented by Chemical Formula 1:

wherein, in Chemical Formula 1,

Ar 3 is a cyclic group represented by Chemical Formula 2A:

wherein, in Chemical Formula 2A,

Y 1 is one of N or CR a ,

wherein R a is one of hydrogen, deuterium, or a substituted or unsubstituted C1 to C10 alkyl group,

R 11 , R 12 , R 13 , R 14 , and R 15 are one of hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C4 to C30 heteroaryl group, a halogen, a cyano group (—CN), a cyano-containing group, or a combination thereof, or R 12 and R 13 and R 14 and R 15 are independently link with each other to provide an aromatic ring,

m1 is 0 or 1,

n in Chemical Formula 2A is 0 or 1, and

* is a linking point,

R 1 to R 3 are independently one of hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen, a cyano group (—CN), a cyano-containing group, or a combination thereof,

R 1 and R 2 independently are present or linked with each other to provide a ring,

Ar 1 and Ar 2 are independently one of a substituted or unsubstituted C6 to C30 arene group, a substituted or unsubstituted C3 to C30 heteroarene group, or a combination thereof in a condensed ring, and

G is one of —(CR d R e ) n —, —O—, —S—, —Se—, —N═, —NR f —, —SiR g R h —, —SiR gg R hh —, —GeR i R j —, —GeR ii R jj , —(C(R m )═C(R n ))—, —(C(R mm )═C(R nn ))—, or a single bond, wherein R d , R e , R f , R g , R h , R i , R j , R m , and R n are independently one of hydrogen, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, wherein R gg , R hh , R ii , R jj , R mm , and R nn are independently one of a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, and at least one pair of R gg and R hh , R ii and R jj , or R mm and R nn are linked with each other to provide a ring structure, and

n in —(CR d R e ) n — is 1 or 2.

2. The compound of claim 1 , wherein in Chemical Formula 1,

at least one of Ar 1 and Ar 2 includes a heteroatom at No. 1 position, and

the heteroatom is one of nitrogen (N), sulfur (S), or selenium (Se).

3. The compound of claim 1 , wherein an electron donor moiety of the N-containing hetero aromatic ring in Chemical Formula 1 is represented by Chemical Formula 4A:

wherein, in Chemical Formula 4A,

G is one of —(CR d R e ) n —, —O—, —S—, —Se—, —N═, —NR f —, —SiR g R h —, —SiR gg R hh —, —GeR i R j —, —GeR ii R jj —, —(C(R m )═C(R n ))—, —(C(R mm )═C(R nn ))—, or a single bond, wherein R d , R e , R f , R g , R h , R i , R j , R m , and R n are independently one of hydrogen, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, wherein R gg , R hh , R ii , R jj , R mm , and R nn are independently one of a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, and at least one pair of R gg and R hh , R ii and R jj , or R mm and R nn are linked with each other to provide a ring structure, and n in —(CR d R e ) n — is 1 or 2, and

R 4a to R 4d and R 5a to R 5d are independently one of hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen, a cyano group (—CN), a cyano-containing group, or a combination thereof, or

two adjacent groups of R 4a to R 4d are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring, or two adjacent groups of R 5a to R 5d are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring.

4. The compound of claim 1 , wherein an electron donor moiety of the N-containing hetero aromatic ring in Chemical Formula 1 is represented by Chemical Formula 4B:

wherein, in Chemical Formula 4B,

G is one of —(CR d R e ) n —, —O—, —S—, —Se—, —N═, —NR f —, —SiR g R h —, —SiR gg R hh —, —GeR i R j —, —GeR ii R jj —, —(C(R m )═C(R n ))—, —(C(R mm )═C(R nn ))— or a single bond wherein R d , R e , R f , R g , R h , R i , R j , R m , and R n are independently one of hydrogen, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, wherein R gg , R hh , R ii , R jj , R mm , and R nn are independently one of a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, and at least one pair of R gg and R hh , R ii and R jj , or R mm and R nn are linked with each other to provide a ring structure, and n in —(CR d R e ) n — is 1 or 2, and

R 4a to R 4d and R 5b to R 5d are independently one of hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen, a cyano group (—CN), a cyano-containing group, or a combination thereof, or

two adjacent groups of R 4a to R 4d are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring, or two adjacent groups of R 5b to R 5d are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring.

5. The compound of claim 1 , wherein an electron donor moiety of the N-containing hetero aromatic ring in Chemical Formula 1 is represented by Chemical Formula 4C:

wherein, in Chemical Formula 4C,

G is one of —(CR d R e ) n , —O—, —S—, —Se—, —N═, —NR f —, —SiR g R h —, —SiR gg R hh —, —GeR i R j —, —GeR ii R jj —, —(C(R m )═C(R n ))—, —(C(R mm )═C(R nn ))— or a single bond wherein R d , R e , R f , R g , R h , R i , R j , R m , and R n are independently one of hydrogen, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, wherein R gg , R hh , R ii , R jj , R mm , and R nn are independently one of a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, and at least one pair of R gg and R hh , R ii and R jj , or R mm and R nn are linked with each other to provide a ring structure, and n in —(CR d R e ) n — is 1 or 2, and

R 4b to R 4d and R 5b to R 5d are independently one of hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen, a cyano group (—CN), a cyano-containing group, or a combination thereof, or

two adjacent groups of R 4b to R 4d are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring, or two adjacent groups of R 5b to R 5d are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring.

6. The compound of claim 1 , wherein an electron donor moiety of the N-containing hetero aromatic ring in Chemical Formula 1 is represented by Chemical Formula 4D:

wherein, in Chemical Formula 4D,

G is one of —(CR d R e ) n , —O—, —S—, —Se—, —N═, —NR f —, —SiR g R h —, —SiR gg R hh —, —GeR i R j —, —GeR ii R jj —, —(C(R m )═C(R n ))—, —(C(R mm )═C(R nn ))— or a single bond wherein R d , R e , R f , R g , R h , R i , R j , R m , and R n are independently one of hydrogen, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, wherein R gg , R hh , R ii , R jj , R mm , and R nn are independently one of a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, and at least one pair of R gg and R hh , R ii and R jj , or R mm and R nn are linked with each other to provide a ring structure, and n in —(CR d R e ) n — is 1 or 2, and

R 4a to R 4d and R 5b and R 5d are independently one of hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen, a cyano group (—CN), a cyano-containing group, or a combination thereof, or

two adjacent groups of R 4a to R 4d are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring.

7. The compound of claim 1 , wherein an electron donor moiety of the N-containing hetero aromatic ring in Chemical Formula 1 is represented by Chemical Formula 4E:

wherein, in Chemical Formula 4E,

G is one of —(CR d R e ) n , —O—, —S—, —Se—, —N═, —NR f —, —SiR g R h —, —SiR gg R hh —, —GeR i R j —, —GeR ii R jj —, —(C(R m )═C(R n ))—, —(C(R mm )═C(R nn ))— or a single bond wherein R d , R e , R f , R g , R h , R i , R j , R m , and R n are independently one of hydrogen, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, wherein R gg , R hh , R ii , R jj , R mm , and R nn are independently one of a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C10 aryl group, and at least one pair of R gg and R hh , R ii and R jj , or R mm and R nn are linked with each other to provide a ring structure, and n in —(CR d R e ) n — is 1 or 2, and

R 4a to R 4d and R 5b and R 5c are independently one of hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen, a cyano group (—CN), a cyano-containing group, or a combination thereof, or

two adjacent groups of R 4a to R 4d are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring, or two adjacent groups of R 5b and R 5c are linked with each other to provide a 5-membered aromatic ring or a 6-membered aromatic ring.

8. The compound of claim 1 , wherein the compound has a maximum absorption wavelength (λ max ) in a wavelength region of greater than or equal to about 500 nm and less than or equal to about 600 nm.

9. The compound of claim 1 , wherein the compound exhibits a light absorption curve having a full width at half maximum (FWHM) of about 50 nm to about 120 nm, in a thin film state.

10. The compound of claim 1 , wherein a difference between a melting point of the compound and a deposition temperature at which 10 wt % of an initial weight of the compound is lost is greater than or equal to about 3° C.

11. A photoelectric device, comprising

a first electrode and a second electrode facing each other, and

an active layer between the first electrode and the second electrode, wherein

the active layer includes the compound of claim 1 .

12. An image sensor comprising:

the photoelectric device of claim 11 .

13. The image sensor of claim 12 , wherein

the image sensor includes a semiconductor substrate and a photoelectric device on the semiconductor substrate,

the semiconductor substrate is integrated with a plurality of first photo-sensing devices configured to sense light in a blue wavelength region and a plurality of second photo-sensing devices configured to sense light in a red wavelength region, and

the photoelectric device is configured to selectively sense light in a green wavelength region, and

the photoelectric device is the photoelectric device of claim 11 .

14. The image sensor of claim 13 , further comprising:

a color filter layer on the semiconductor substrate, wherein

the color filter layer includes a blue filter and a red filter, the blue filter is configured to selectively transmit light in a blue wavelength region, and the red filter is configured to selectively transmit light in a red wavelength region.

15. The image sensor of claim 13 , wherein the first photo-sensing devices and the second photo-sensing devices are stacked in a vertical direction in the semiconductor substrate.

16. The image sensor of claim 12 , wherein

the photoelectric device is a green photoelectric device,

the image sensor includes a blue photoelectric device configured to selectively absorb light in a blue wavelength region, the image sensor includes a red photoelectric device configured to selectively absorb light in a red wavelength region, and the green photoelectric device, the blue photoelectric device, and the red photoelectric device are stacked.

17. An electronic device comprising:

the image sensor of claim 12 .